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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37015생성일: 2026년 10월 25일

Dimethylformamide → 3-Acetylthio-1-(N-p-nitrobenzyloxycarbonylacetimidoyl)pyrrolidine

https://huagongshe.com/reaction/37015

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Sodium hydrideHCID 24758—
반응물3-Methanesulphonyloxy-1-(N-p-nitrobenzyloxycarbonylacetimidoyl)pyrrolidineHCID 53997171—
반응물HCID 178418634HCID 178418634—
용매WaterHCID 962—
생성물3-Acetylthio-1-(N-p-nitrobenzyloxycarbonylacetimidoyl)pyrrolidineHCID 5403714579.1%

반응 단계

To 300 ml of anhydrous N,N-dimethylformamide were added 7.35 g of sodium hydride in the form of a 55% w/w/ dispersion in oil, followed by 12.5 g of thioacetic acid. The mixture was then stirred for 10 minutes, with ice-cooling, after which 40 g of 3-methanesulphonyloxy-1-(N-p-nitrobenzyloxycarbonylacetimidoyl)pyrrolidine were added. The mixture was then stirred for 3 hours at 65° C. After the reaction mixture had been allowed to cool, water was added and the mixture was extracted with ethyl acetate. The extract was washed with water and dried and then the solvent was distilled off under reduced pressure. The residue was purified by chromatography through a column of silica gel, eluted with a 2:1 by volume mixture of benzene and ethyl acetate, to give 30 g of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE034960
출처 데이터셋uspto-grants-1995_05
ORD IDord-10b960678bc34a7c81eff1c395c66e14
출처 메모uspto-grants-1995_05