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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1533505생성일: 2026년 10월 26일

Glycine → (R)-2-benzylbutyrolactone

https://huagongshe.com/reaction/1533505

반응식

참여 물질

역할이름HCID투입량
반응물GlycineHCID 750—
반응물NadideHCID 5892—
반응물Sodium HydroxideHCID 14798—
반응물4-MethoxybenzaldehydeHCID 31244—
반응물2-Benzylbutane-1,4-diolHCID 13428547—
용매AcetoneHCID 180—
용매EthanolHCID 702—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물(R)-2-benzylbutyrolactoneHCID 11355800—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06207862B1
출처 데이터셋uspto-grants-2001_03
ORD IDord-c1c93d3a972c4fc09ed3da79d0d49b93
출처 메모uspto-grants-2001_03