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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1795026생성일: 2026년 10월 25일

Sodium borohydride → (5-(4-(Trifluoromethyl)phenyl)-4,5-dihydroisoxazol-3-yl)methanol

https://huagongshe.com/reaction/1795026

반응식

참여 물질

역할이름HCID투입량
반응물Sodium borohydrideHCID 4311764—
반응물Ethyl 5-(4-(trifluoromethyl)phenyl)-4,5-dihydroisoxazole-3-carboxylateHCID 22064077—
용매EthanolHCID 702—
생성물(5-(4-(Trifluoromethyl)phenyl)-4,5-dihydroisoxazol-3-yl)methanolHCID 2218476078%

반응 단계

To a stirred mixture of sodium borohydride (378 mg, 10.0 mmol) in ethanol (20 ml) was added slowly a solution of ethyl 5-(4-(trifluoromethyl)phenyl)-4,5-dihydroisoxazole-3-carboxylate (1.6 g, 5.75 mmol) in ethanol (10 mL). The resulting reaction mixture was stirred under an atmosphere of nitrogen for 8 hours. Ethanol was removed under reduced pressure and water (20 ml) added. The aqueous mixture was acidified to about pH 3 with concentrated HCl, and the acidic solution extracted with ethyl acetate (3×20 ml). The resulting organic phase was washed with saturated aqueous sodium bicarbonate (20 ml), 30% aqueous ammonium chloride(20 ml), brine, dried over sodium-sulfate, concentrated, and purified using chromatography (3% MeOH in CH2Cl2) to afford (5-(4-(trifluoromethyl)phenyl)-4,5-dihydroisoxazol-3-yl)methanol (1.1 g, M+1=246.1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07026321B2
출처 데이터셋uspto-grants-2006_04
ORD IDord-462b83e0aa924d4bb79f599a9119fbea
출처 메모uspto-grants-2006_04