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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 468548생성일: 2026년 10월 26일

Sodium Chloride → 3-Ethoxybenzo[D]isoxazol-6-OL

https://huagongshe.com/reaction/468548

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물Boron tribromideHCID 25134—
반응물1,2-BenzisoxazoleHCID 71073—
반응물Sodium BicarbonateHCID 516892—
반응물3-Ethoxy-6-methoxybenzo[D]isoxazoleHCID 21077805—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매Ethyl acetate hexaneHCID 21226206—
생성물3-Ethoxybenzo[D]isoxazol-6-OLHCID 135848745—

반응 단계

Boron tribromide (1.0M solution in dichloromethane; 1.39 ml, 1.39 mmol) was added to a stirred, −78° cooled solution of benzisoxazole from part (c) (179 mg, 928 μmol) in dichloromethane (4 ml) under an argon atmosphere. The reaction mixture was gradually warmed to room temperature over approx. 2 hours, and stirred overnight. Tlc (silica, 2:1 hexane/ethyl acetate) showed new polar material as well as unreacted starting material. The reaction was worked up by adding water (5 ml) and ice. The aqueous phase was neutralized by addition of saturated NaHCO3 solution, and saturated with NaCl. The aqueous phase was extracted into dichloromethane (3×60 ml), then the organic extracts combined and washed with brine (10 ml) and dried (NaSO4). The product was purified by chromatography on silica (18 g; eluent 2.5%, 5%, then 15% ethyl acetate/hexane). The first compound to elute was unreacted 3-ethoxy-6-methoxy-1,2-benzisoxazole, (46 mg), followed by 3-ethoxy-6-hydroxy-1,2-benzisoxazole 108 mg (65%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08624025B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-e14487a2cb074265b850a55d99405b4a
출처 메모uspto-grants-2014_01