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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416862Generated: October 25, 2026

Glycine → (R)-2-benzylbutyrolactone

https://huagongshe.com/reaction/1416862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycineHCID 750—
ReactantNadideHCID 5892—
ReactantSodium HydroxideHCID 14798—
Reactant4-MethoxybenzaldehydeHCID 31244—
Reactant2-Benzylbutane-1,4-diolHCID 13428547—
SolventAcetoneHCID 180—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(R)-2-benzylbutyrolactoneHCID 11355800—

Reaction Steps

Glycine (18.8 grams) is dissolved in 2 liters of deionized water, and the pH is adjusted by the addition of 10% sodium hydroxide to 9.0. 2-Benzyl-1,4-butanediol (10.0 grams) is dissolved in 150 ml of acetone added to the glycine solution with stirring, followed by the addition of β-NAD+ (Sigma, 0.5 grams). To the resulting solution is added horse liver alcohol dehydrogenase (Sigma, 250 mg, approximately 400 units). After the enzyme has dissolved the pH is readjusted to 9.0 with 10% sodium hydroxide, and the reaction mixture is stirred at 30° C. During the reaction, the pH is maintained at 9.0 with a pH-stat by the addition of 10% sodium hydroxide. Progress of the reaction is monitored by thin layer chromatography (Silica gel plates, eluent methylene chloride; visualization by dipping in a solution of 5% anisaldehyde in ethanol and heating). When the reaction is complete as judged by thin layer chromatography, the reaction mixture is adjusted to a pH of 13 with 10 M sodium hydroxide and then extracted 3 times with 250 ml of methylene chloride. The pH of the aqueous mixture is then adjusted to 3 with concentrated HCl, followed by continuous extraction with 1 liter of ethyl acetate for 24 hours. The ethyl acetate extract is dried over anhydrous magnesium sulfate and evaporated under reduced pressure to yield (R)-2-benzylbutyrolactone as a yellowish solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05916786
Source datasetuspto-grants-1999_06
ORD IDord-0340abcfe284489fa1f078a24d667d33
Source noteuspto-grants-1999_06