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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1388292생성일: 2026년 10월 27일

Hydrochloric Acid → Ammonium Hydroxide

https://huagongshe.com/reaction/1388292

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물S-benzyl-L-cysteineHCID 193613—
반응물Ethyl alpha-oxobenzenebutanoateHCID 562087—
반응물Sodium cyanoborohydrideHCID 5003444—
용매EthanolHCID 702—
생성물Ammonium HydroxideHCID 149237%
생성물N-[1(S)-carboethoxy-3-phenylpropyl]-S-benzyl-(R)-cysteineHCID 22825650—

반응 단계

Stir 10.5 g of S-benzyl-L-cysteine and 11.0 g of 2-oxo-4-phenylbutyric acid, ethyl ester in 1000 ml of absolute ethanol at room temperature for 24 hours. Add 5.28 g of sodium cyanoborohydride and stir the resulting mixture at room temperature for 48 hours. Concentrate this mixture in vacuo at 30° C. to give a white residue. Suspend the residue in ice-water, add concentrated hydrochloric acid to maintain pH 2-4, and stir this mixture for 11/2-2 hours. Absorb this aqueous solution on XAD-2 (Rohm & Haas Co.) resin. Elute the resin with water and then with absolute ethanol. Concentrate the ethanol solution and chromatograph the residue on a column of silica gel using chloroform:isopropanol:7% ammonium hydroxide 1:1:1 (organic layer) to give N-[1(S)-carboethoxy-3-phenylpropyl]-S-benzyl-(R)-cysteine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04431645
출처 데이터셋uspto-grants-1984_02
ORD IDord-76903b21356742eb90462bc9e69eb91e
출처 메모uspto-grants-1984_02