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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Trifluoroacetic acid | HCID 6422 | — |
| 반응물 | Benzyl(methoxymethyl)((trimethylsilyl)methyl)amine | HCID 353442 | — |
| 반응물 | (R)-3-methacryloyl-4-phenyloxazolidin-2-one | HCID 677330 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | (R)-3-((S)-1-benzyl-3-methylpyrrolidine-3-carbonyl)-4-phenyloxazolidin-2-one | HCID 70983198 | 683.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08889704B2 |
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| 출처 데이터셋 | uspto-grants-2014_11 |
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| ORD ID | ord-02446b8d51614e65beb02f4f717ac37d |
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| 출처 메모 | uspto-grants-2014_11 |
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