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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 501628생성일: 2026년 10월 25일

tert-Butyl-(2S,3R)-3-{[tert-butyl(dimethyl)silyl]oxy}-2-formylpyrrolidine-1-carboxylate → (2R,3R)-3-(tert-Butyl-dimethylsilanyloxy)-2-[(1S)-(1-hydroxy-2-methylpropyl)]pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/501628

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참여 물질

역할이름HCID투입량
반응물tert-Butyl-(2S,3R)-3-{[tert-butyl(dimethyl)silyl]oxy}-2-formylpyrrolidine-1-carboxylateHCID 16732142—
반응물HCID 178418918HCID 178418918—
용매TetrahydrofuranHCID 8028—
생성물(2R,3R)-3-(tert-Butyl-dimethylsilanyloxy)-2-[(1S)-(1-hydroxy-2-methylpropyl)]pyrrolidine-1-carboxylic acid tert-butyl esterHCID 6845944279.8%

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온도-60 °C

반응 단계

To 51C (6.50 g, 19.8 mmol) in THF (100 mL) at −78° C. was added a 2M THF solution of isopropylmagnesium chloride (30.0 mL, 60.0 mmol) over 20 min. The cold bath was removed and the reaction was stirred for 1 h. The reaction was then cooled to −60° C. and was quenched with saturated aqueous ammonium chloride. After warming to rt, the whole was diluted with EtOAc. The layers were separated and the organic layer washed with water and brine, then dried (MgSO4), filtered and concentrated. The resulting residue was purified via flash chromatography eluting with 20% EtOAc/hexane to provide the title compound (5.90 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772267B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-dd743f4e10864eb89f05085eabffc2f4
출처 메모uspto-grants-2010_08