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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2073265생성일: 2026년 10월 26일

Sodium hydride → 4-(4-Chlorophenylsulfonylamino)pyrrolidine

https://huagongshe.com/reaction/2073265

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물SodiumHCID 5360545—
반응물(2S,4R)-1-t-butoxycarbonyl-4-(4-chlorophenylsulfonylamino)-2-formylpyrrolidineHCID 15670377—
반응물(4-Carboxy-4-methylpentyl)triphenylphosphonium bromideHCID 19858212—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물4-(4-Chlorophenylsulfonylamino)pyrrolidineHCID 17914505—

반응 단계

To a solution of (4-carboxy-4-methylpentyl)triphenylphosphonium bromide (3.83 g) in dimethyl sulfoxide (21 ml) was added sodium methylsulfinylmethide [19.5 m mol, prepared from sodium hydride (468 mg) and dimethyl sulfoxide (17 ml)]and the solution was stirred at room temperature for 30 minutes. To the resulting solution was added (2S,4R)-1-t-butoxycarbonyl-4-(4-chlorophenylsulfonylamino)-2-formylpyrrolidine (1.0 g) in dimethyl sulfoxide (3.0 ml) and the mixture was stirred at room temperature for 1 hour. After addition of water (50 ml), the solution was washed with ethyl acetate and the aqueous layer was adjusted to pH 1 with 1N hydrochloric acid. The aqueous solution was extracted with ethyl acetate and the organic phase was washed successively with water and brine. The solution was dried over magnesium sulfate and the solvent was evaporated in vacuo to give (2S,4R)-1-t-butoxycarbonyl-2-[(E and Z)-5-carboxy-5-methyl-1-hexenyl]-4-(4-chlorophenylsulfonylamino)pyrrolidine as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04916152
출처 데이터셋uspto-grants-1990_04
ORD IDord-221c7f04ce9e43ffb8ab60ef971428d6
출처 메모uspto-grants-1990_04