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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1994070생성일: 2026년 10월 26일

Sodium hydride → (R)-1-[3-(t-butyl-dimethyl-silanyloxy)-phenyl-sulfanylcarbonyl]-pyrrolidine-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1994070

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물3-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]benzenethiolHCID 21976868—
반응물HCID 86605608HCID 86605608—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물(R)-1-[3-(t-butyl-dimethyl-silanyloxy)-phenyl-sulfanylcarbonyl]-pyrrolidine-2-carboxylic acid ethyl esterHCID 86605607—

반응 단계

To a stirred suspension of sodium hydride (0.25 g, 6.3 mmol) in anhydrous THF (20 mL) is added 3-(t-butyl-dimethyl-silanyloxy)-benzenethiol (1.3 g, 5.22 mmol) at RT. After 10 min, the title A compound, (R)-1-chlorocarbonyl-pyrrolidine-2-carboxylic acid ethyl ester (1.1 g, 5.22 mmol) is added and the reaction is stirred for 24 h. The reaction mixture is diluted with ethyl acetate, washed with water and brine, dried over anhydrous magnesium sulfate and concentrated at reduced pressure. The crude product is purified on a Biotage 40M column using 25% ethyl acetate in hexane to yield (R)-1-[3-(t-butyl-dimethyl-silanyloxy)-phenyl-sulfanylcarbonyl]-pyrrolidine-2-carboxylic acid ethyl ester as a clear oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07652061B2
출처 데이터셋uspto-grants-2010_01
ORD IDord-63dac54499cf4f5886219bbcb17ac26d
출처 메모uspto-grants-2010_01