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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13185생성일: 2026년 10월 24일

Cesium fluoride → 1,1,1-trifluoro-3-(1-(4-fluorophenyl)-1H-indazol-5-yloxy)-3-phenylpropane-2,2-diol

https://huagongshe.com/ko/reaction/13185

반응식

참여 물질

역할이름HCID투입량
반응물Cesium fluorideHCID 25953—
반응물(Trifluoromethyl)trimethylsilaneHCID 552549—
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물methyl 2-(1-(4-fluorophenyl)-1H-indazol-5-yloxy)-2-phenylacetateHCID 59339649—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물1,1,1-trifluoro-3-(1-(4-fluorophenyl)-1H-indazol-5-yloxy)-3-phenylpropane-2,2-diolHCID 5933973696%

반응 단계

Methyl 2-(1-(4-fluorophenyl)-1H-indazol-5-yloxy)-2-phenylacetate (147d, 2.5 g, 6.6 mmol) was dissolved in THF (15 mL, dried over 4 Å MS) under Argon atmosphere and cooled in an ice-bath. Trimethyl(trifluoromethyl)silane (1.18 mL, 8 mmol) was added followed by Caesium fluoride (100 mg, 0.66 mmol). The cooling bath was removed and the stirring was continued at r.t. for 4 h. A solution of tetrabutylammonium fluoride in THF (1M, 7 mL, 7 mmol) followed by water (4 mL) was then added and the mixture was stirred for additional 1 h and then partitioned between ethyl acetate and water. The organic phase was washed twice with water, then brine and evaporated to afford 1,1,1-trifluoro-3-(1-(4-fluorophenyl)-1H-indazol-5-yloxy)-3-phenylpropane-2,2-diol (2.74 g, 95%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728030B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-f9ae0f6d3dd046ca8cdda5139a80df1d
출처 메모uspto-grants-2010_06