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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 734415생성일: 2026년 10월 25일

Water → 7-Propyl-3-(trifluoromethyl)benzo[d]isoxazol-6-ol

https://huagongshe.com/reaction/734415

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물1-(2,4-Dihydroxy-3-propylphenyl)-2,2,2-trifluoroethanone oximeHCID 136340076—
용매TetrahydrofuranHCID 8028—
생성물7-Propyl-3-(trifluoromethyl)benzo[d]isoxazol-6-olHCID 135800812—

반응 조건

온도0 °C

반응 단계

1-(2,4-Dihydroxy-3-propylphenyl)-2,2,2-trifluoroethanone oxime (prepared by the method described in WO 97/28137, 4.2 g, 15.96 mmol) and triphenylphosphine (8.82 g, 33.6 mmol) were dissolved in THF (250 mL) and the mixture was cooled to 0° C. A solution of diethyl azodicarboxylate (5.02 mL, 32.0 mmol) in THF (150 mL) was then slowly added over a period of 30 minutes. The reaction mixture was stirred for 1 h at 0° C. After addition of water (500 mL), the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with brine and dried over sodium sulfate. The solvent was removed in vacuo and the product purified via silica gel flash chromatography (ethyl acetate/hexane (v/v)=1:6). The product was obtained as a white-yellow powder in a yield of 1.96 g (8.0 mmol, 50%). 1H NMR (300 MHz, CDCl3) δ 1.00 (t, 3H), 1.73 (m, 2H), 2.88 (t, 2H), 5.34 (s, 1H), 6.93 (d, 1H), 7.48 (d, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07592361B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-30116643c65e41a4885b89270ce4adee
출처 메모uspto-grants-2009_09