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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 338825생성일: 2026년 10월 26일

Trifluoroacetic acid → (R)-3-((S)-1-benzyl-3-methylpyrrolidine-3-carbonyl)-4-phenyloxazolidin-2-one

https://huagongshe.com/reaction/338825

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Benzyl(methoxymethyl)((trimethylsilyl)methyl)amineHCID 353442—
반응물(R)-3-methacryloyl-4-phenyloxazolidin-2-oneHCID 677330—
용매TolueneHCID 1140—
생성물(R)-3-((S)-1-benzyl-3-methylpyrrolidine-3-carbonyl)-4-phenyloxazolidin-2-oneHCID 70983198683.5%

반응 단계

To a solution of (R)-3-methacryloyl-4-phenyloxazolidin-2-one (135.00 g, 583.79 mmol) and TFA (4.497 mL, 58.379 mmol) in dry toluene (50 mL) at <10° C. was quickly added dropwise N-benzyl-1-methoxy-N-((trimethylsilyl)methyl)methanamine (194.16 mL, 758.93 mmol), and the mixture was stirred at ambient temperature overnight. The reaction was filtered and the filtrate was extracted with 4N HCl (3×250 mL). The aqueous layer was washed with ethyl acetate (250 mL) then made basic with solid K2CO3 to pH 10. The basic aqueous layer was extracted with ethyl acetate (4×400 mL), dried (MgSO4), filtered and concentrated under reduced pressure to provide (R)-3-((S)-1-benzyl-3-methylpyrrolidine-3-carbonyl)-4-phenyloxazolidin-2-one (145 g, 399 mmol, 68% yield) as a dark oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889704B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-02446b8d51614e65beb02f4f717ac37d
출처 메모uspto-grants-2014_11