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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

반응식

참여 물질

역할이름HCID투입량
반응물3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, (S)-(-)-HCID 179824—
반응물(Trifluoromethyl)trimethylsilaneHCID 552549—
반응물Tetrabutylammonium FluorideHCID 2724141—
촉매Tetrabutylammonium FluorideHCID 2724141—
용매TetrahydrofuranHCID 8028—
생성물(S)-tert-butyl 2,2-dimethyl-4-(2,2,2-trifluoro-1-hydroxyethyl)oxazolidine-3-carboxylateHCID 1094647792.7%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642632B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-93324d6f5b2344c5b14a673db5d4e78e
출처 메모uspto-grants-2014_02