4.
6: Step-by-Step Procedures For Extractions
1.
Single Extraction
Figur
e 4.20: Progress of the extraction of methyl red (the colored compound) from the acidic aqueous
layer (bottom) into the organic layer (top). The inversions were done slowly in order to see the
extraction stepwise. With even gentle mixing, the methyl red extracts rapidly.
The pictures in this section show a single extraction of methyl red (colored compound, Figure
4.21) from an aqueous solution (bottom layer) into 25mL25mL of ethyl acetate (top layer).
The aqueous solution originally has a pink color, as the methyl red appears red in acidic solution
(the aqueous solution was made from 50mL50mL water, 5 drops
of 0.1MHCl0.1MHCl and 5 drops of 1%1% methyl red indicator solution). The methyl red
has a large partition coefficient and is extracted from the aqueous layer into the ethyl acetate in
this process.
Figure 4.21: Structure of methyl red in
highly acidic solution.
Fig
ure 4.22: Organic chemistry students using separatory funnels.
Figure 4.23: a) Separatory funnel, b) Correct order of stopcock components, c) Glass stopcock,
d) Funnel in cushioned ring clamp.
Prepare the Setup (for single extraction)
1. Obtain a separatory funnel (Figure 4.23a).
a. If the separatory funnel has a Teflon stopcock, reassemble the stopcock if it was taken
apart to dry, placing the parts in the appropriate order (Figure 4.23b). Be sure that the
Teflon stopcock is moderately tight so that it can still easily turn, but is not so loose that
liquid can seep around the joint.
b. If using a glass stopcock (Figure 4.23c), it likely needs no further preparation. There
should be a very thin layer of grease used to seal the stopcock and prevent freezing. If
both glass and Teflon stopcocks are available, Teflon is a better choice as there is always
a possibility that solvent can dissolve the grease used with glass stopcocks and
contaminate the sample.
c. Also obtain a stopper (Teflon or ground glass) that fits well in the top joint of the funnel
(Figure 4.23a).
2. Place the separatory funnel in a ring clamp attached to a ring stand or latticework. The
funnels are easy to break, so cushion the funnel in the metal clamp using pieces of slit
rubber or plastic tubing (Figure 4.23d).
Figure 4.24: a) Closed and open stopcocks, b) Pouring in liquid with a funnel: notice the
Erlenmeyer flask positioned below as a fail-safe, c) Pouring in the organic solvent, d) Separatory
funnel before mixing.
Add the Solutions (for single extraction)
3. Before pouring anything into a separatory funnel, be sure that the stopcock is in the
"closed" position, where the stopcock is horizontal (Figure 4.24a).
As a fail-safe, always position an Erlenmeyer flask beneath the separatory funnel before
pouring (Figure 4.24b). This can catch liquid in case the stopcock is accidentally left
open, or if the stopcock is loose and liquid leaks through unintentionally.
4. Using a funnel, pour the liquid to be extracted into the separatory funnel (Figures 4.24b +
4.25). A separatory funnel should never be used with a hot or warm liquid.
The ground glass joint atop a separatory funnel is more prone to stick to the stopper if
there was liquid in the joint at some point. Pouring liquid into the separatory funnel using
a short-stemmed funnel avoids getting the joint wet, so that it will be less likely to freeze
during mixing.
Figure 4.25: Student adds liquid to a
separatory funnel.
5. Pour a quantity of the extractive solvent into the separatory funnel, as indicated by the
procedure (Figure 4.24c).
It is unnecessary to use precise quantities of solvent for extractions, and the volumes can
be measured in a graduated cylinder. If a procedure calls for 20mL20mL of solvent, it
is acceptable if between 2020-25mL25mL is used each time.
Figure 4.26: a) Holding the separatory funnel before shaking, b) Inverting the funnel to mix the
components, c) Venting to release pressure.
Mix the Solutions (for single extraction)
6. Place the stopper on the funnel, and hold the funnel such that the fingers of one hand
securely cover the stopper, while the other hand grips the bottom of the funnel (Figure
4.26a).
7. Gently invert the funnel (Figure 4.26b), and swirl the mixture a little.
Although it is not uncommon for some liquid to creep into the ground glass joint when
inverted, it should be minimal. If liquid drips onto your fingers or gloves when you invert
the funnel, the stopper is probably the wrong size.
8. Pressure may build up inside the separatory funnel when solutions are mixed, so
immediately after swirling, and with the funnel still inverted, "vent" the funnel by briefly
opening the stopcock to allow for a release of pressure (Figure 4.26c).
additional vapor to the initial ∼∼1 atmosphere of air pressure in the funnel. With highly
Pressure builds in the funnel as solvent evaporates into the headspace and contributes
volatile solvents (like diethyl ether), a definite "swoosh" can be heard upon venting, and
small amounts of liquid may even sputter out the stopcock. If liquid spits out the
stopcock, try to allow it to drain back into the funnel. The noise associated with venting
normally ceases after the second or third inversions, as the headspace becomes saturated
with solvent vapors and the pressures inside and outside the funnel are equalized.
Safety note: Never point the stopcock toward someone as you vent, as it's possible some
liquid may splatter onto him or her.
9. Close the stopcock and mix the solutions a bit more vigorously, periodically stopping to
vent the system.
There are differences of opinion on how vigorously solutions should be mixed in
separatory funnels, and for how long. As a general guide, a mild mixing for 10-20
seconds should be enough. With some solutions (e.g. dichloromethane), care should be
taken to not shake too vigorously, as these solutions often form emulsions (where the
interface between the solutions doesn't clarify). With solutions prone to emulsions, a
funnel should be gently rocked for one minute.
10. Place the separatory funnel upright in the ring clamp to allow the layers to fully separate.
The interface between the layers should settle rather quickly, often within 10 seconds or
so. If the interface is clouded or not well defined (an emulsion has formed), see the
troubleshooting section for tips.
Figure 4.27: a) Taking the stopper off before draining the funnel, b) Draining to the interface, c)
Clinging droplets (using a different system), d) Stopping when the interface is in the stopcock.
Separate the Layers (for single extraction)
11. Liquid will not drain well from a separatory funnel if the stopper remains on, as air
cannot enter the funnel to replace the displaced liquid. If liquid did drain from the funnel
without replacement by an equal volume of air, a negative pressure would form in the
funnel. Thus, before draining liquid from a separatory funnel, remove the stopper (Figure
4.27a).
12. Drain the majority of the bottom layer into a clean Erlenmeyer flask, positioning the ring
clamp so that the tip of the separatory funnel is nestled in the Erlenmeyer flask to prevent
splashing (Figure 4.27b). Stop draining when the interface is within 1cm1cm of the
bottom of the stopcock.
13. Gently swirl the funnel to dislodge any droplets clinging to the glass (Figure 4.27c). A
glass stirring rod can be used to knock down stubborn clinging droplets.
14. Further drain the bottom layer, stopping when the interface just enters the stopcock
chamber (Figure 4.27d). Label the Erlenmeyer flask (e.g. "bottom layer").
When labeling flasks, it's often best to use terminology that is without question correct,
such as "top layer" or "bottom layer". If the layers are labeled with statements like
"organic layer" or "aqueous layer", it's possible that the layers have been incorrectly
identified. It may be best to use combined statements like "top organic layer" as it's quite
useful to track the aqueous and organic layers. If the layers have been incorrectly
identified, at least the "top" part of the label will always be correct.
Flasks can be labeled using labeling tape or by writing directly on the glass with a
permanent marker (e.g. Sharpie). Marker ink can be removed from glass by rubbing it
with a KimWipe moistened with a bit of acetone.
Figure 4.28: a) Pouring out the top layer, b) Labeled layers, c) Drying the separatory funnel with
a disassembled stopcock.
15. Pour out the top layer from the top of the separatory funnel into another clean Erlenmeyer
flask (Figure 4.28a), making sure to again label this flask (Figure 4.28b).
It is proper technique to drain the bottom layer through the stopcock, and to pour out the
top layer from the top of the funnel. This method minimizes re-mixing the solutions, as
only the lower layer touches the stem of the funnel.
16. Never throw away any liquids from an extraction until you are absolutely sure that
you have the desired compound. Undesired layers can be properly disposed of when the
desired compound is in your hands (e.g. after the rotary evaporator has removed the
solvent).
Mistakes made during extractions (e.g. carrying on with the wrong layer), can be solved
as long as the solutions have not been placed in the waste container! The layers should
also be saved until after evaporation because the desired compound may not be very
soluble in the solvent used. If the compound failed to extract in one solvent, a different
solvent could be tried later, again only if the layers had not yet been thrown away.
Clean Up (for single extraction)
17. To clean a separatory funnel, first rinse it with acetone into a waste container. Then wash
the funnel with soap and water at your benchtop. Disassemble the Teflon stopcock (if
used). After rinsing with distilled water, allow the parts to dry separated in your locker
(Figure 4.28c).
Single Extraction Summary
Table 4.3: Procedural summary for s
Retur
Use slit tubing to cushion the the rin
separatory funnel in the ring clamp. layers
Hold the separatory funnel so that
Close the stopcock on the separatory Remo
your fingers firmly cover the
funnel and position an Erlenmeyer drain
stopper.
flask beneath the setup, in case it
drips. Drain
Invert the funnel and shake gently
layer
for 10-20 seconds.
Into the separatory funnel pour the
liquid to be extracted using a funnel: Stop w
Periodically "vent" the funnel (open
this prevents liquid from getting on the bo
the stopcock while inverted to
the ground glass joint which can and s
release pressure). Never point the
cause it to stick. drople
tip at someone while venting.
Pour the extractive solvent into the Drain
funnel. stopp
inside
Multiple Extractions
Organic Layer is on the Top
In this section are stepwise instructions on how to extract an aqueous solution with an organic
solvent that is less dense than water (the organic layer will be on the top). As an example, the
instructions are written to extract an aqueous solution three times using 25mL25mL diethyl
ether each time (3×25mL3×25mL diethyl ether). A procedural summary of the first two
extractions is in Figure 4.29.
Figure 4.29: Two extractions when the organic layer is on the top.
Extraction #1
1. Perform a single extraction using approximately 25mL25mL of diethyl ether (an exact
amount is not necessary), as described previously, making sure to appropriately label
each layer (e.g. "top organic layer" and "bottom aqueous layer").
Extraction #2
2. Return the aqueous layer to the separatory funnel. There is no need to wash the funnel in
between extractions.
3. Add a fresh 25mL25mL portion of diethyl ether to the separatory funnel. Stopper the
funnel, invert and shake with venting, then allow the layers to separate.
At this step, there should be two layers in the separatory funnel. If two layers aren't
present, it's likely that the wrong layer was added to the funnel in step 2 (a common
mistake). One way to test if this was the mistake is to add a bit of water from a squirt
bottle. If the layer returned to the separatory funnel is the organic layer (incorrect), the
squirt bottle water will not mix with the solution, and will instead fall as droplets to the
bottom.
If the organic layer (incorrect) was accidentally returned to the separatory funnel, there is
no harm done, as the organic layer was simply diluted. Pour the liquid back into the flask
designed for the organic layer, and instead add the aqueous solution to the funnel.
4. Drain the bottom aqueous layer into an Erlenmeyer flask: it is acceptable to use the same
flask that was used for the aqueous layer in the first extraction (that may have been
labeled "bottom aqueous layer").
5. Since it is most common to combine the organic layers in multiple extractions, the top
organic layer can be poured out of the separatory funnel into the same flask that was used
for the organic layer in the first extraction (that may have been labeled "top organic
layer"). In this flask, there should be roughly 50mL50mL of diethyl ether from the two
extractions.
Extraction #3
6. Repeat the extraction a third time by adding the aqueous layer from the second extraction
into the separatory funnel, followed by another fresh 25mL25mL portion of diethyl
ether. Stopper the funnel, invert and shake with venting, then allow the layers to separate.
7. Drain the aqueous layer into the appropriate flask, and again pour the top layer into the
organic layer flask, where there should be roughly 75mL75mL of diethyl ether from
the three extractions.
Organic Layer is on the Bottom
In this section are stepwise instructions on how to extract an aqueous solution with an organic
solvent that is denser than water (the organic layer will be on the bottom). As an example, the
instructions are written to extract an aqueous solution three times
using 25mLCH2Cl225mLCH2Cl2 each time (3×25mLCH2Cl23×25mLCH2Cl2,
Figure 4.30).
Figure 4.30: Two extractions when the organic layer is on the bottom.
Extraction #1
1. Perform a single extraction using approximately 25mL25mL of dichloromethane
(CH2Cl2CH2Cl2, an exact amount is not necessary), as described previously, with the
following differences:
a. As CH2Cl2CH2Cl2 is prone to emulsions, invert the funnel and shake gently for one
minute with venting.
b. After allowing the layers to separate in the funnel, drain the bottom organic layer into a
clean Erlenmeyer flask (and label the flask, e.g. "bottom organic layer"). Do not drain the
top aqueous layer from the funnel.
Extraction #2
2. To the aqueous layer remaining in the funnel, add a fresh 25mL25mL portion of
dichloromethane. Stopper the funnel, invert and shake gently for 1 minute with venting,
then allow the layers to separate.
3. Since it is most common to combine the organic layers in multiple extractions, the
bottom organic layer can be drained from the separatory funnel into the same flask that
was used for the organic layer in the first extraction (that may have been labeled "bottom
organic layer"). In this flask, there should be roughly 50mL50mL of dichloromethane
from the two extractions.
Extraction #3
4. Repeat the extraction by adding another fresh 25mL25mL portion of dichloromethane
to the aqueous layer in the separatory funnel. Stopper the funnel, invert and shake gently
with venting, then allow the layers to separate.
5. Drain the bottom organic layer into the flask used previously, where there should be
roughly 75mL75mL of dichloromethane from the three extractions.
Troubleshooting
This section descries common problems and solutions in extractions.
There is Only One Layer
The most common reason for having only one layer in a separatory funnel when there should be
two (as in when the procedure tells you to "separate the layers"), is to have made a mistake.
What likely happened is that the wrong layer was added to the separatory funnel - for example
the organic layer was unknowingly added instead of the aqueous layer. When organic solvent is
added to an organic layer in the separatory funnel, the result is only one layer. The mistake can
be remedied as long as the layers have not yet been thrown away! If the correct layer is added to
the funnel, everything will work out as planned.
To prevent making this mistake in the future, be sure to label the Erlenmeyer flasks. Also, be
sure to never throw away a layer until you are absolutely sure that you've done everything
correctly.
An occasional reason that only one layer forms in a separatory funnel is if there are large
quantities of compounds present that dissolve in both solvents, for example if large amounts of
ethanol are present, which dissolve well in both aqueous and organic solvents. In this situation,
the best approach is to remove the troublesome compound (i.e. the ethanol) on a rotary
evaporator before extraction.
There are Three Layers
The most common reason for three layers in a separatory funnel is inadequate mixing (Figure
4.31a). If the funnel is shaken with more vigor it will likely settle into two layers (Figure 4.31b).
It is also possible that a middle third layer is an emulsion, where the two layers are not fully
separated.
Figure 4.31: a)
Three initial layers from inadequate mixing, b) Two layers resulting from more vigorous mixing.
There is Insoluble Material at the Interface
A small amount of insoluble film between two layers is not uncommon during an extraction.
Polymeric materials tend to rest between layers as solvent interactions are minimized at the
interface. A minor film is not something to worry about because if a small amount does make it
into the organic layer, a subsequent drying and filtration step will often remove it.
The Interface Cannot be Seen
On occasion the compounds in a separatory funnel are so dark that they obscure the interface
between the two layers. If this happens, there are several methods that might help you see the
interface. One is to hold the separatory funnel up to the light, or to shine a flashlight onto the
glass (Figure 4.32b). Additional light sometimes allows you to see the interface. A second
method is to carefully observe the layers while tilting the funnel back and forth to the side
(Figure 4.32c). Your eye can sometimes pick up on subtle differences in the way the liquids
flow. A third method is to add a bit more solvent to the funnel to somewhat dilute one of the
layers, or to add a different solvent to alter the index of refraction.
Figure 4.32: a) Interface is too dark to easily see, b) Flashlight visualizes the interface, c) Tilting
also subtly visualizes the interface, although it is much less dramatic.
The Layers Don't Separate Well (An Emulsion Formed)
Emulsions are when tiny droplets of one layer are suspended in the other layer, resulting in no
distinct interface between the two layers (Figure 4.33). Often an emulsion looks like a bubbly
mess near the interface, and can even appear to be an odd-looking third layer.
Figure 4.33: Emulsion formed between
dichloromethane and brine (with food coloring).
Emulsions can happen for several reasons:
1. The density of each layer may be so similar that there is weak motivation for the liquids
to separate.
2. There may be soap-like compounds or other emulsifying agents present that dissolve
some of the components in one another.
Figure 4.34: a) An emulsion with biodiesel and methanol, b) An emulsion with brine and ethyl
acetate, c) An emulsion with dichloromethane and brine (as well as food coloring), d) The
emulsion is resolved after addition of water that decreases the density of the top brine layer.
Emulsions can be very difficult to rectify, and it's best if they are avoided in the first place by
shaking solutions that are prone to emulsions (e.g. dichloromethane with highly basic or dense
solutions) gently in the separatory funnel. Nonetheless, if an emulsion does form, there are some
ways to attempt to clarify them:
a. For mild emulsions, gently swirl the layers and try to knock down suspended droplets
with a glass stirring rod.
b. Allow the solution to sit for a period of time (even until the next lab period) if possible.
With enough time, some solutions do settle out on their own. This of course may not be
practical.
c. For small volumes, use a centrifuge if one is available. A centrifuge hastens the process
of letting an emulsion settle on its own. Remember that a centrifuge needs to be balanced
or it may wobble off the benchtop. Divide the solutions equally, putting tubes of equal
volume opposite one another inside the centrifuge.
d. If an emulsion is formed because the two layers have similar densities, try to alter the
density of each layer to make them more different. To help clarify an emulsion, try to
decrease the density of the top layer or increase the density of the bottom layer.
For example, if an emulsion occurs with ethyl acetate (top layer) and an aqueous solution
(bottom layer), add some NaClNaCl. NaClNaCl will dissolve in the aqueous layer
and increase the density of the aqueous solution. Alternatively add additional ethyl
acetate, which will dilute the organic layer and lower its density. As a last resort add
some pentane, which will mix with the top organic layer and decrease its density (pentane
is one of the least dense organic solvents). The addition of pentane is used as a final effort
as it will negatively affect the ability of the organic layer to extract somewhat polar
compounds.
If an emulsion occurs with an aqueous solution (top layer) and dichloromethane (bottom
layer), add some water from a squirt bottle to dilute the top layer and decrease its density.
This method worked well to clarify the emulsion in Figure 4.32c, as evidenced by Figure
4.32d.
e. Try decreasing the solubility of one component in the other. One method is to
add NaClNaCl or NH4ClNH4Cl to the separatory funnel, which dissolves in the
aqueous layer and decreases the ability of organic compounds to dissolve in water
("salting out").
Microscale Extractions
Microscale work involves the manipulation of less than 300mg300mg of compound, and
usually involves solvent volumes of 5mL5mL or less. A separatory funnel would be
impractical when working with such small quantities, and conical vials (Figure 4.35) or
centrifuge tubes are typically used instead.
Figure 4.35: Progress of the extraction of methyl red from the acidic aqueous layer (bottom) into
the organic layer (top). The inversions were done very slowly in order to see the extractions
stepwise. With even gentle mixing the methyl red (and thus color) extracts rapidly.
The pictures in this section show the extraction of 2mL2mL of a mildly acidic aqueous
solution containing a single drop of methyl red solution into 2mL2mL of ethyl acetate. The
color (methyl red), is extracted from the aqueous layer (bottom) into the ethyl acetate layer (top).
Figure 4.36: a) Adding solvent to the conical vial by pipette, and using a beaker to support the
vial, b) Supporting the vial with a cork ring, c+d) Attaching the Teflon-lined cap to the vial, e)
Manual mixing of layers (using a different system).
Mix the Solutions (for microscale extraction)
1. Pour the contents to be extracted into a conical vial, or a glass tube with a tapered end
(e.g. centrifuge tube). As these containers are prone to tip, use a beaker (Figure 4.36a) or
inverted cork ring (Figure 4.36b) for support.
2. Add the extractive solvent by pipette (Figure 4.36a). If using a conical vial, the volume
markings on the glass may be helpful.
3. Gently mix the two solutions using one of the following methods:
a. Secure a cap firmly on the vial (Figure 4.36c+d) then invert and shake the tube for 10-20
seconds (Figure 4.35). Conical vials and centrifuge tubes tend to be less airtight than
separatory funnels, so there should be no need to vent the system during shaking
unless NaHCO3NaHCO3 or Na2CO3Na2CO3 solutions are used.
b. Alternatively, manually mix the layers using a pipette. Withdraw a pipette-full of the
bottom layer from the vial, and then vigorously expunge the solution through the top
layer (Figure 4.36e). Do this repeatedly for at least one minute. Manual mixing is not
recommended when using low-boiling solvents (e.g. diethyl ether), as the volume often
decreases dramatically after mixing. Instead use the first mixing method described.
Figure 4.37: a+b) Withdrawal of the bottom layer, with pipette into the tip of the vial, c)
Removal of a residual drop of the bottom layer by allowing the layers to separate inside a Pasteur
pipette, d) Separated layers.
Separate the Layers (for microscale extraction)
4. Separate the layers with a Pasteur pipette. The design of conical vials and centrifuge
tubes allows for efficient separation of the layers through withdrawal of the bottom layer
by pipette. This means that even if the top layer is to be reserved, the bottom layer still
needs to be removed first.
a. Hold the conical vial or tapered tube in the same hand as a container for the bottom layer
(label it). Withdraw the majority of the bottom layer by Pasteur pipette, and dispense into
the container (Figure 4.37a).
b. When withdrawing, always place the pipette tip to the point of the conical vial or tapered
tube (Figure 4.37b).
c. It may be difficult to remove the very last drop of bottom layer from the point of the vial.
To do so, withdraw the entirety of the bottom layer and a small amount of the top layer
into the pipette. Allow the layers to separate inside the pipette (Figure 4.37c), then
delicately expel the bottom layer from the pipette into the container. Return the rest of the
top layer to the conical vial.
5. If the bottom layer is the desired layer, and another extraction is to be done, add fresh
organic solvent to the top layer still in the conical vial and repeat the extraction and
separation.
6. If the top layer is the desired layer, remove it from the conical vial using a fresh pipette
into a clean container. If another extraction is to be done, return the bottom layer to the
conical vial, add fresh solvent and repeat the extraction and separation.
This page titled 4.6: Step-by-Step Procedures For Extractions is shared under a CC BY-NC-ND
4.0 license and was authored, remixed, and/or curated by Lisa Nichols via source content that
was edited to the style and standards of the LibreTexts platform.
1. Back to top
2.
o 4.5: Extraction Theory
o 4.7: Reaction Work-Ups
Was this article helpful?
Yes
No
?
The LibreTexts libraries are Powered by NICE CXone Expert and are
supported by the Department of Education Open Textbook Pilot Project, the
UC Davis Office of the Provost, the UC Davis Library, the California State
University Affordable Learning Solutions Program, and Merlot. We also
acknowledge previous National Science Foundation support under grant
numbers 1246120, 1525057, and 1413739. Legal. Accessibility
Statement For more information contact us at info@[Link].
contentsreadabilityresourcestools
Complete your gift to make an impact
