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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 657712생성일: 2026년 10월 27일

Trifluoroacetic acid → (S)-3-((3R,4S)-1-benzyl-4-phenyl-pyrrolidine-3-carbonyl)-4-phenyl-oxazolidin-2-one

https://huagongshe.com/reaction/657712

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Benzyl(methoxymethyl)((trimethylsilyl)methyl)amineHCID 353442—
반응물Sodium BicarbonateHCID 516892—
반응물(4S)-4-Phenyl-3-(3-phenylprop-2-enoyl)-1,3-oxazolidin-2-oneHCID 679769—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
생성물(S)-3-((3R,4S)-1-benzyl-4-phenyl-pyrrolidine-3-carbonyl)-4-phenyl-oxazolidin-2-oneHCID 5453941564.7%

반응 단계

N-Benzyl-N-(methoxymethyl)trimethylsilylmethylamine (10.03 g, 40.5 mmol) was added to (S)-4-phenyl-3-[(E)-(3-phenyl-acryloyl)]-oxazolidin-2-one (10.3 g, 35.1 mmol) in toluene (150 mL) at 0° C. and stirred for 20 minutes. Trifluoroacetic acid (9.7 mL) in dichloromethane (125 mL) was added dropwise to the reaction mixture keeping the internal temperature at 0° C. The reaction was stirred at room temperature overnight. The reaction mixture was poured into saturated sodium bicarbonate (200 mL) and extracted with dichloromethane (2×75 mL). The combined organic phases were washed with brine and dried over sodium sulfate. The organic phases were concentrated to give a waxy solid, which was purified by flash silica gel chromatography eluting with ethyl acetate:hexanes (1:9) to give 9.68 g (61%) of (S)-3-((3R,4S)-1-benzyl-4-phenyl-pyrrolidine-3-carbonyl)-4-phenyl-oxazolidin-2-one.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08076349B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-7db2a4b899d547ae9bf15a5580b6d335
출처 메모uspto-grants-2011_12