Download Chemistry 3719L – Week 9 Reduction of Benzil with Sodium

Spring 2004
Chemistry 3719L – Week 9
Reduction of Benzil with Sodium Borohydride
Pre-lab reading from Zubrick:
Chapter 13:
Chapter 12:
Whole Chapter – review recrystallization
Pages 87-92 – review melting points
Aims
The use of metal hydride reagents (e.g. NaBH4 and LiAlH4) for the reduction of aldehydes and
ketones is the most widely used method for conversion to primary and secondary alcohols respectively.
This experiment will give you experience in using the milder NaBH4 reagent that readily converts the
diketone benzil into the corresponding diol hydrobenzoin.
Reaction
Benzil (1) is treated with sodium borohydride (NaBH4, 2) to give the diol hydrobenzoin (3) via a
nucleophilic addition reaction. Since the NaBH4 reaction is much less basic than LiAlH4 we can run the
reaction in a protic solvent such as ethanol, which also serves as the proton source to generate the final
alcohol product.
.
OH
O
NaBH4 (2)
O
EtOH
1
OH
3
Procedure
• In a 125 mL Erlenmeyer flask add benzil (1.5 g) and 95% ethanol (15 mL). Cool the flask under
running water such that the benzyl forms a fine suspension in the ethanol.
• Weigh out sodium borohydride (0.3 g – careful, this fine powder is dangerous if accidentally
inhaled) and add this to the reaction mixture in one portion.
• Swirl the flask gently for 15 minutes, making notes about any color or temperature changes.
• Carefully add DI water (15 mL) and bring the mixture to a boil. If the mixture is not clear then
gravity filter it whilst hot into a second Erlenmeyer flask.
• Add more DI water (~30 mL) to the filtrate and allow the solid to crystallize (scratching the glass
with a glass rod might help here).
• Filter the solid, dry for 15 minutes then weigh the product and obtain the melting point.
• If possible you should obtain an IR spectrum of your product to compare with that of the benzil
starting material. This information will be used in your report to prove that the functional group
conversion (i.e. ketone to alcohol) actually occurred.
• You should hand the product to your TA in a sealed, labeled test tube for grading.
Synthesis Report = 10 pts
Adapted from Williamson, Macroscale and Microscale Organic Experiments, Houghton Mifflin.