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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13431생성일: 2026년 10월 25일

Imidazole → (2R,4R)-4-(tert-butyl-diphenyl-silanyloxy)-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester

https://huagongshe.com/reaction/13431

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물DimethylformamideHCID 6228—
반응물tert-ButyldiphenylchlorosilaneHCID 94078—
반응물(2R,4R)-1-((benzyloxy)carbonyl)-4-hydroxypyrrolidine-2-carboxylic acidHCID 688416—
용매Ethyl AcetateHCID 8857—
생성물(2R,4R)-4-(tert-butyl-diphenyl-silanyloxy)-pyrrolidine-1,2-dicarboxylic acid 1-benzyl esterHCID 67482921—

반응 단계

2.32 g of tert-butyldiphenylsilyl chloride and 2.32 g of imidazole were added in order to a dimethylformamide (60 ml) solution of 3.61 g of (2R,4R)-4-hydroxy-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester, and the reaction liquid was stirred overnight at room temperature. The reaction liquid was diluted with ethyl acetate, washed with aqueous saturated ammonium chloride and saturated saline in order, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=1/2) to obtain the entitled compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728025B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-72690fe8b46b401484ce85a4f574b9e7
출처 메모uspto-grants-2010_06