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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37251생성일: 2026년 10월 24일

Ethyl Acetate → (2S,4R)-4-methanesulfonyloxy-2-(thiazol-4-yl)-1-(4-nitrobenzyloxycarbonyl)pyrrolidine

https://huagongshe.com/ko/reaction/37251

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물MethanethioamideHCID 3005587—
반응물(2S,4R)-2-bromoacetyl-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidineHCID 14305067—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물(2S,4R)-4-methanesulfonyloxy-2-(thiazol-4-yl)-1-(4-nitrobenzyloxycarbonyl)pyrrolidineHCID 1430507588%

반응 단계

To a mixture of (2S, 4R)-2-bromoacetyl-4-methane-sulfonyloxy-1- (4-nitrobenzyloxycarbonyl)pyrrolidine(1.15 g) in a mixture of methanol (20 ml) and dichloromethane (15 ml) was added thioformamide (453 mg) at room temperature. After stirring at the same temperature for 4 hours, the mixture was poured into ethyl acetate and washed in turn with saturated aqueous sodium bicarbonate and brine. The dried organic layer was evaporated and the resulting oil was crystallized from a mixture of n-hexane and dichloromethane (100:1 V/V) to give (2S, 4R) -4-methanesulfonyloxy-2-(thiazol-4-yl)-1- (4-nitrobenzyloxycarbonyl)pyrrolidine (930 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420122
출처 데이터셋uspto-grants-1995_05
ORD IDord-023370ae923f417cb88f524b72199bb7
출처 메모uspto-grants-1995_05