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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 603378생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/603378

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriphenylphosphineHCID 11776—
반응물Diethyl azodicarboxylateHCID 5462977—
반응물1-(2,4-Dihydroxy-3-propylphenyl)-2,2,2-trifluoroethanone oximeHCID 136340076—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물7-Propyl-3-(trifluoromethyl)benzo[d]isoxazol-6-olHCID 13580081250%

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온도0 °C

반응 단계

1-(2,4-Dihydroxy-3-propylphenyl)-2,2,2-trifluoroethanone oxime (4.2 g, 15.96 mmol, prepared by the method described in WO9728137) and PPh3 (8.82 g, 33.6 mmol) were dissolved in THF (250 mL), and the mixture was cooled to 0° C. A solution of DEAD (5.02 mL, 32.0 mmol) in THF (150 mL) was slowly added over a period of 30 min. The reaction mixture was stirred for 1 h at 0° C. After addition of water (500 mL) and extraction with EtOAc (3×300 mL), the combined organic phases were washed with brine (300 mL), dried over Na2SO4, filtered, and concentrated under reduced pressure. The product was purified by silica gel flash chromatography (1:6 EtOAc/hexane) to yield 1.96 g (50%) of the title compound as a light yellow powder. 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 번호US07906653B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-83ffd2f5ab7c4aedbb33add5f1d566ba
출처 메모uspto-grants-2011_03