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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1710237생성일: 2026년 10월 26일

2-Ethoxy-2-hydroxyacetic acid p-nitrobenzyl ester → 2-[(3S,4R)-4-acetylthio-3-methoxy-2-oxoazetidin-1-yl]-2-hydroxyacetic acid p-nitrobenzyl ester

https://huagongshe.com/reaction/1710237

반응식

참여 물질

역할이름HCID투입량
반응물2-Ethoxy-2-hydroxyacetic acid p-nitrobenzyl esterHCID 11043316—
반응물(3S,4R)-4-acetylthio-3-methoxy-2-oxoazetidineHCID 56630779—
용매TolueneHCID 1140—
용매DimethylformamideHCID 6228—
생성물2-[(3S,4R)-4-acetylthio-3-methoxy-2-oxoazetidin-1-yl]-2-hydroxyacetic acid p-nitrobenzyl esterHCID 56607651—

반응 단계

714 mg of 2-ethoxy-2-hydroxyacetic acid p-nitrobenzyl ester and 4 g of molecular sieve A4 are added to a solution of 245 mg of (3S,4R)-4-acetylthio-3-methoxy-2-oxoazetidine in a mixture of 8 ml of toluene and 2 ml of dimethylformamide and the mixture is stirred overnight at room temperature. The molecular sieves are filtered off from the mixture and the filtrate is concentrated by evaporation in vacuo. The residue is chromatographed over silica gel, and by elution with toluene/ethyl acetate (9:1 and 4:1) the title compound, contaminated with some glyoxylate, is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04952690
출처 데이터셋uspto-grants-1990_08
ORD IDord-a4e360f1257f4fb4867c6c83b38cf7fd
출처 메모uspto-grants-1990_08