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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1693072생성일: 2026년 10월 27일

Hydrochloric Acid → 2-(6-Bromoquinolin-2-yl)-1,1,1-trifluoropropan-2-ol

https://huagongshe.com/reaction/1693072

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물(Trifluoromethyl)trimethylsilaneHCID 552549—
반응물1-(6-Bromoquinolin-2-yl)ethanoneHCID 57458165—
촉매Tetrabutylammonium FluorideHCID 2724141—
용매DimethylformamideHCID 6228—
생성물2-(6-Bromoquinolin-2-yl)-1,1,1-trifluoropropan-2-olHCID 57458166105.1%

반응 단계

A DMF (5 ml) solution of 1-(6-bromoquinolin-2-yl)ethanone (129 mg, 0.52 mmol), (trifluoromethyl)trimethylsilane (220 mg, 1.55 mmol) and tetrabutylammonium fluoride (13.5 mg, 0.052 mmol) was stirred at 100° C. for 2 hours. Then the mixture was cooled to room temperature and 1N-hydrochloride aqueous solution (2 ml) was added. After 4 hours, the mixture was quenched with saturated sodium bicarbonate aqueous solution, and the product was extracted with ethyl acetate which was dried over sodium sulfate. Then, filtration, evaporation and purification through silica gel column chromatography, eluting with hexane/ethyl acetate (4:1), furnished the title compound (175 mg, quant.) as a white solid. 1H NMR (300 MHz, CDCl3) δ 1.81 (3H, s), 6.51 (1H, s), 7.64 (1H, d, J=8.1 Hz), 7.66-7.89 (1H, m), 8.00-8.12 (2H, m), 8.21 (1H, d, J=8.8 Hz). MS (ESI): m/z 320, 322 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08158650B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-28786fdef50f42f7923fb0988b47e921
출처 메모uspto-grants-2012_04