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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 657713생성일: 2026년 10월 24일

Water → ((3R,4S)-1-Benzyl-4-phenylpyrrolidin-3-YL)methanol

https://huagongshe.com/ko/reaction/657713

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Aluminium lithium hydrideHCID 21226445—
반응물(S)-3-((3R,4S)-1-benzyl-4-phenyl-pyrrolidine-3-carbonyl)-4-phenyl-oxazolidin-2-oneHCID 54539415—
용매TetrahydrofuranHCID 8028—
생성물((3R,4S)-1-Benzyl-4-phenylpyrrolidin-3-YL)methanolHCID 2134104755%

반응 단계

To (S)-3-((3R,4S)-1-benzyl-4-phenyl-pyrrolidine-3-carbonyl)-4-phenyl-oxazolidin-2-one (9.96 g, 23.35 mmol) in THF (100 mL) in a three-necked flask equipped with a thermometer and addition funnel was added lithium aluminium hydride (48 mL, 1M in THF) dropwise so that the temperature did not exceed 40° C. while keeping the reaction vessel in a water bath. When addition was complete the water bath was removed and the reaction stirred at room temperature overnight. The reaction was carefully quenched with water (1.6 mL), NaOH (1.6 mL, 2N) and water (4.5 mL). After stirring for 15 minutes, the reaction mixture was filtered through a pad of celite and rinsed with THF (40 mL). The filtrate was concentrated to give a pale yellow oil, which was purified by flash silica gel chromatography eluting with ethyl acetate:hexanes (1:1) to give 3.38 g (55%) of ((3R,4S)-1-benzyl-4-phenyl-pyrrolidin-3-yl)-methanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08076349B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-299cec936e7a4442bd43484ed4c37e26
출처 메모uspto-grants-2011_12