Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238572생성일: 2026년 10월 27일
3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, (S)-(-)- → (S)-tert-butyl 2,2-dimethyl-4-(2,2,2-trifluoro-1-hydroxyethyl)oxazolidine-3-carboxylate
https://huagongshe.com/reaction/238572
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, (S)-(-)- | HCID 179824 | — |
| 반응물 | (Trifluoromethyl)trimethylsilane | HCID 552549 | — |
| 반응물 | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| 촉매 | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (S)-tert-butyl 2,2-dimethyl-4-(2,2,2-trifluoro-1-hydroxyethyl)oxazolidine-3-carboxylate | HCID 10946477 | 92.7% |
반응 단계
To a mixture of (S)-4-formyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (1.0 g, 4.36 mmol), (trifluoromethyl)trimethylsilane (2.0 M solution in THF, 2.6 mL, 5.20 mmol) in THF (10 mL) was added tetrabutylammonium fluoride (1.0 M solution in THF, 0.1 mL, 0.10 mmol) at 0° C. After addition, the mixture was stirred at room temperature for 60 h. Then, tetrabutylammonium fluoride (1.0 M solution in THF, 9 mL, 9.0 mmol) was added and the mixture stirred for another 6 h and subsequently quenched by adding saturated aq. NaHCO3 solution, extracted with EtOAc. The extracts were washed with saturated aq. NaHCO3 solution, water, brine and dried over Na2SO4. Concentration and purification gave (S)-tert-butyl 2,2-dimethyl-4-(2,2,2-trifluoro-1-hydroxyethyl)oxazolidine-3-carboxylate (1.21 g, 92%), which showed a complicated NMR spectrum because of the different comformers.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08642632B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-93324d6f5b2344c5b14a673db5d4e78e |
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| 출처 메모 | uspto-grants-2014_02 |
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