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Analysis of Aspirin
Acetylsalicylic acid is the chemical name for aspirin, the ubiquitous pain reliever. One of the
compounds used in the synthesis of aspirin is salicylic acid, which is itself a pain reliever that
was known to many ancient cultures, including the Native Americans who extracted it from
willow tree bark. Salicylic acid is extremely bitter tasting, and frequent use can cause severe
stomach irritation. The search for a milder form of this pain reliever led to the successful
synthesis of acetylsalicylic acid by the German chemist Felix Hoffmann in 1893.
Your two primary objectives in this experiment will be to synthesize and analyze aspirin. There
is more than one way to synthesize aspirin; in this experiment, you will react acetic anhydride
with salicylic acid in the presence of phosphoric acid (which acts as a catalyst). The reaction
equation is shown below.
HO
HO
O
O
OH
+
Salicylic acid
H3C
O
O
H 3P O
CH3
Acetic anhydride
O
O
(a q )
CH3
Acetylsalicylic acid
H3C
OH
Acetic acid
You will conduct two tests of your synthesis to verify that you did indeed make aspirin, and to
determine its relative purity. First, you will measure the melting temperature of a sample of your
product, using a Melt Station. Second, you will use a Spectrophotometer to test the absorbance of
salicylic acid impurity in your aspirin sample after it has been complexed with Fe3+ from
iron (III) nitrate solution.
OBJECTIVES
In this experiment, you will
MATERIALS
Part I Synthesis Materials
50 mL Erlenmeyer flask
two 10 mL graduated cylinders
25 mL graduated cylinder
250 mL beaker
Bchner funnel, filter, and filter paper
spoon, spatula, or rubber policeman
ice bath
hot plate
plastic Beral pipet or eyedropper
salicylic acid
aspirin crystals (from Part I)
ethanol, denatured
0.025 M iron (III) nitrate solution, Fe(NO3)3
distilled water
100 mL volumetric flask
250 mL volumetric flask
PROCEDURE
Part I Synthesize Aspirin
1. Obtain and wear goggles. Protect your arms and hands by wearing a long-sleeve lab coat and
gloves. Conduct this reaction in a fume hood.
2. Measure out 2.0 g of salicylic acid into a 50 mL Erlenmeyer flask.
3. Add 5.0 mL of acetic anhydride and 5 drops of 85% phosphoric acid solution. Swirl the
mixture. If necessary, use a sparingly small amount of distilled water to rinse down any bits
of solid that may be on the inner walls of the flask. CAUTION: Handle the phosphoric acid
and acetic anhydride with care. Both substances can cause painful burns if they come in
contact with the skin.
4. You are now ready to begin the synthesis of aspirin.
a. Prepare a 7080C hot-water bath using a 250 mL beaker on a hot plate. Monitor the
water temperature using a Temperature Probe or thermometer.
b. Hold and partially submerge the 50 mL flask and contents in the water bath.
c. Heat the mixture in the hot-water bath for 15 minutes, or until the mixture ceases releasing
vapors. Stir the mixture occasionally during heating. Add 2 mL of distilled water about
10 minutes into the heating.
c. Carefully observe your sample. When the solid begins to melt, click Mark to mark the
temperature on your graph (or press the D key on the computer or the OK button on
LabQuest). When the entire solid has completely melted, click Mark again. The two
values marked on your graph describe the estimated melting temperature range of your
substance.
d. When you have determined the approximate melting temperature range for the sample,
stop data collection. Store the run by tapping the File Cabinet icon in LabQuest, or
choosing Store Latest Run from the Experiment menu in Logger Pro. Discard the
capillary tube and sample as directed by your instructor.
e. On the Melt Station, turn the control knob to the Fan/Cooling setting to get ready for the
next trial. The blue light will turn on indicating that the fan is cooling the Melt Station.
13. Now that you have a rough idea of the melting temperature, a more accurate determination of
the melting temperature can be made. Use a previously prepared sample in a capillary tube,
as described in Step 8, to determine the melting temperature of the sample:
a. Start data collection.
b. On the Melt Station, turn the control knob to the Rapid Heat setting.
c. Carefully observe the temperature vs. time graph. When the temperature is within
approximately 10C of the lowest possible melting temperature of your sample, turn the
control knob to a temperature setting corresponding to your expected melting temperature.
d. Carefully observe your sample. When the solid begins to melt, click Mark to mark the
temperature on your graph. When the entire solid has completely melted, click Mark
again. The two values marked on your graph describe the estimated melting temperature
range of your substance. When you are finished with this step, stop data collection.
e. Store the run.
f. Discard the capillary tube and sample as directed by your instructor.
g. On the Melt Station, turn the control knob to the Fan/Cooling setting to get ready for the
next trial.
14. Repeat Step 13 until you have determined the melting temperature range of your aspirin.
Record the melting temperature range in your data table.
15. At the end of your testing, turn the control knob on the Melt Station to Off.
Part III Test the Spectrophotometric Absorbance of an Aspirin Sample
Your synthesis converted most, but not all, of the salicylic acid into acetylsalicylic acid. You will
mix iron (III) nitrate with salicylic acid in your aspirin sample to complex the salicylic acid,
which is a bluish-purple color. You will analyze several samples to determine the amount of
salicylic acid impurity in your synthesized aspirin. You can use this information to calculate the
purity of your aspirin sample. Follow Steps 1621 to prepare a set of salicylic acid standard
solutions and conduct testing to develop your own Beers law plot of the standards. Steps 2225
will guide you through the set up and testing of your aspirin sample.
16. Quantitatively prepare the stock salicylic acid solution.
a. Measure out about 0.20 g of salicylic acid. Record the mass, to the nearest 0.001 g.
b. Transfer the salicylic acid to a 250 mL beaker and add 10 mL of ethanol. Swirl the beaker
to dissolve the solid.
c. Add 150 mL of distilled water to the beaker. Mix the solution.
Standard salicylic
acid solution from
Step 17 ab (mL)
Water
(mL)
1
2
3
4
5
10.0
8.0
6.0
4.0
2.0
0
2.0
4.0
6.0
8.0
18. Disconnect the Melt Station and connect the Spectrophotometer to the USB port of LabQuest
or a computer. Start the data-collection program, then choose New from the File menu.
19. Calibrate the Spectrophotometer.
a. To prepare a blank cuvette, fill a cuvette 3/4 full with 0.025 M Fe(NO3)3 solution. Place
the blank cuvette in the Spectrophotometer.
b. Choose Calibrate from the Sensors menu of LabQuest or the Experiment menu of
Logger Pro.
c. When the warmup period is complete, select Finish Calibration. Select OK.
20. Determine the optimal wavelength for creating the standard curve and set up the mode of
data collection.
a. Empty the Fe(NO3)3 solution from the blank cuvette. Using the solution in the 100 mL
volumetric flask of salicylic acid (Trial 1), rinse the cuvette twice with ~1 mL amounts,
and then fill it 3/4 full. Wipe the outside with a tissue and place it in the
Spectrophotometer.
b. Start data collection. A full spectrum graph of the solution will be displayed. Stop data
collection. The wavelength of maximum absorbance ( max) is automatically identified.
c. Change the mode to Events with Entry (absorbance vs. concentration) and select a
wavelength for analysis:
In Logger Pro, click the Configure Spectrometer button, . Click Abs vs. Concentration
as the Collection Mode. The wavelength of maximum absorbance ( max) will be selected.
21. You are now ready to collect data for the five standard solutions.
a. Leave the Trial 1 cuvette in the Spectrophotometer and start data collection.
b. When the absorbance value displayed on the screen has stabilized, select Keep and enter
the molar concentration. Select OK. The absorbance and concentration values have now
been saved for the first solution.
c. Discard the cuvette contents as directed by your instructor. Using the solution in the
second 100 mL volumetric flask, rinse the cuvette twice with ~1 mL amounts, and then fill
it 3/4 full. Wipe the outside, place it in the device, and close the lid. After closing the lid,
wait for the absorbance to stabilize and select Keep. Enter the molar concentration, and
select OK.
d. Repeat the procedure for the remaining salicylic acid solutions that you prepared.
e. Stop data collection to view a graph of absorbance vs. concentration.
f. Record the absorbance and concentration values in your data table. You can do this either
by examining your data points along the curve, or by viewing the data table.
g. Choose Curve Fit from the Analyze menu.
h. Choose Linear as the Fit Equation. Select OK. The graph should indicate a direct
relationship between absorbance and concentration, a relationship known as Beers law.
The regression line should closely fit the five data points and pass through (or near) the
origin of the graph.
i. After the preparation and testing of your aspirin sample in the following steps, you will be
instructed to interpolate along this plot to determine the concentration of salicylic acid
impurity in your aspirin sample.
22. Prepare the synthesized aspirin sample for testing. Complete this step quickly and be ready to
proceed directly to Step 23.
a. Measure out about 0.4 g of aspirin and transfer it to the 250 mL beaker. Record the mass
of aspirin that you use to the nearest 0.01 g.
b. Add 10 mL of ethanol to the beaker of aspirin sample. Swirl the mixture to dissolve the
solid.
c. Add 150 mL of distilled water to the beaker. Mix the solution.
d. Quantitatively transfer the solution from the beaker to a 250 mL volumetric flask.
Thoroughly rinse the beaker with several portions of distilled water, and transfer the rinse
water to the volumetric flask. Add distilled water, as needed, to fill the flask to the 250 mL
mark. Mix the solution thoroughly.
e. Transfer 5 mL of the aspirin solution from the 250 mL volumetric flask to a clean and dry
100 mL volumetric flask. Add 0.025 M Fe(NO3)3 solution to the flask to make precisely
100.0 mL. Mix the solution thoroughly.
DATA TABLE
Part I Synthesis of Aspirin
Mass of salicylic acid used (g)
Volume of acetic anhydride used (mL)
Mass of acetic anhydride (1.08 g/mL) used (g)
Mass of aspirin and filter paper (g)
Mass of filter paper (g)
Mass of aspirin synthesized (g)
Part II Melting Temperature Data
Melting temperature range (C)
Part III Salicylic Acid Standard Stock Solution
Initial mass of salicylic acid (g)
Moles of salicylic acid (mol)
Initial molarity of salicylic acid (mol/L)
Part III Beers Law Data for Salicylic Acid Standard Solutions
Trial
Concentration (mol/L)
Absorbance
1
2
3
4
5
Test of the Purity of the Synthesized Aspirin
Initial mass of aspirin sample (g)
Absorbance of aspirin sample
Concentration of salicylic acid (mol/L)
Moles of salicylic acid in aspirin sample (mol)
Mass of salicylic acid in aspirin sample (g)
Mass of aspirin in sample (g)
Percent aspirin in sample (%)
DATA ANALYSIS
1. What is the theoretical yield of aspirin in your synthesis? The mole ratio is 1:1 between
salicylic acid and acetic anhydride in this reaction.
2. Using a literature source or the internet, find the accepted melting temperature value of pure
acetylsalicylic acid. How does the melting temperature test of your aspirin compare to the
accepted value?
3. Based on the results of the absorbance testing with the Spectrophotometer, what is the
percent purity of your sample of aspirin? Does this percent purity compare well with the
results of the melting temperature test? Explain.
4. Use your percent purity calculations to determine the percent yield of your synthesis of
aspirin.
INSTRUCTOR INFORMATION
1. Each lab team will use about 2 g of salicylic acid.
2. The 0.025 M Fe(NO3)3 solution can be prepared by using 10.10 g of FeNO39H2O per 1 L.
3. The yield for this reaction will be lower than your students expectations. A low yield may
not always be the result of sloppy work, but poor lab technique will certainly result in a
disappointing yield.
4. You may choose to shorten Part III by providing your students with Beers law standards.
5. It is critical for your students to complete the spectrophotometric analysis of their samples
(Part III) in one lab period, because of the instability of the prepped samples.
6. After students complete the Part 1 synthesis, they will need to dry the sample. You may
choose to have them wait until the next lab period, to ensure that the sample is dry. Or, if you
wish to have them complete Parts II and III in the same lab period, you will need to provide
an air-flow supply (low flow) to fairly quickly air dry their aspirin sample.
HAZARD ALERTS
Salicylic acid: Harmful if swallowed. Causes mild skin irritation. Causes serious eye damage.
HMIS Classification: Health hazard2, Flammability0, Physical hazard0.
Acetic anhydride: Strongly irritating and corrosive. Moderate fire risk (flash point 49C).
Causes severe eye damage. Wear eye protection. Have access to eyewash. Vapors are
strongly irritating. Open and dispense in fume hood. Reacts (sometimes delayed) violently
with water. Moderately toxic by ingestion and inhalation. HMIS Classification: Health
hazard3, Flammability2, Physical hazard2.
Phosphoric acid (o-phosphoric acid): Skin and eye irritant. Toxic by ingestion and inhalation.
Burns tissue. HMIS Classification: Health hazard3, Flammability0, Physical hazard0.
Ethanol: Fire risk (flash point 14.0C). Flammable. Addition of denaturant makes the product
poisonous. Store in dedicated flammables cabinet. Skin and eye irritant. Moderately toxic by
ingestion and inhalation. HMIS Classification: Health hazard2, Flammability3, Physical
hazard1.
Iron (III) nitrate: May intensity fire; oxidizer. May be harmful if swallowed. Causes skin
irritation. May cause respiratory irritation. HMIS Classification: Health hazard2,
Flammability0, Physical hazard3.
The hazard information reference is Sigma-Aldrich Co., 1-800-325-3010,
www.sigmaaldrich.com/safety-center/msds-search.html
SAMPLE DATA
Part I Synthesis of Aspirin
Mass of salicylic acid used (g)
2.01
5.0
5.40
2.52
0.56
1.96
132.6133.9
0.201
0.00145
0.00579
Part III Beers Law Data for Salicylic Acid Standard Solutions
Trial
Concentration (mol/L)
Absorbance
5.79 104
1.005
4.63 104
0.832
3.47 104
0.616
2.32 104
0.423
1.16 104
0.211
10
0.40
0.277
1.50 104
1.5 105
0.10
0.30
75
SAMPLE CALCULATIONS
1. For the sample data, the theoretical yield of aspirin is 2.63 g. The calculation is based on
salicylic acid (the limiting reactant),
mol of salicylic acid used = 2.01 g 138.13 g/mol = 0.0146 mol
mol of salicylic acid = mol of aspirin produced (theoretical)
theoretical mass of aspirin produced = 0.0146 mol 180.16 g/mol = 2.63 g
2. The experimentally determined melting temperature of 132.6C compares well with the
accepted melting temperature of pure acetylsalicylic acid, 135C.
3. The results of the spectrophotmetric test show that the percent purity of the synthesized
aspirin is 75%. This compares reasonably well with the melting temperature test.
For the sample data, the calculations are as follows.
The absorbance of the aspirin sample is 0.081. The absorbance of 0.081 equals a salicylic
acid concentration of 1.50 104 mol/L. Because the sample volume is 100 mL, the molar
amount of salicylic acid impurity in the aspirin sample is 1.50 105 mol.
There was 1.50 105 mol of salicylic acid in a 5 mL sample. This 5 mL sample was taken
from 250 mL of solution. Thus, there is (1.50 105 mol (250/5) = 7.50 104 mol of
salicylic acid in the initial aspirin sample. The mass of salicylic acid is:
7.50 104 mol 138.13 g/mol = 0.10 g
The initial mass of the aspirin sample is 0.40 g. If 0.10 g of this sample is unreacted salicylic
acid, then the percent of aspirin in the sample is: (30 g/40 g) 100 = 75%.
4. Answers will vary. For the sample data, the mass of synthesized aspirin is 1.96 g. Corrected
for purity, is: (1.96 0.75) = 1.47 g. The percent yield is: (1.47 g 2.63 g) 100 = 55.9%.
SAMPLE DATA
11
12