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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1094657생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1094657

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DimethylformamideHCID 6228—
반응물(Trifluoromethyl)trimethylsilaneHCID 552549—
반응물Tributylammonium fluorideHCID 11217984—
반응물HCID 86634942HCID 86634942—
생성물2-(6-Bromoquinolin-2-yl)-1,1,1-trifluoropropan-2-olHCID 57458166—

반응 단계

A DMF (5 ml) solution of the 6-bromoquinoline-ethanone (129 mg, 0.52 mmol), (trifluoromethyl)trimethylsilane (220 mg, 1.55 mmol) and tributylammonium fluoride (13.5 mg, 0.052 mmol) was stirred at 100° C. for 2 hours. Then the mixture was cooled to room temperature and added 1M-hydrochloride aqueous solution (2 ml). After 4 hours, the mixture was quenched with saturated sodium bicarbonate aqueous solution, and the product was extracted with ethyl acetate and dried over sodium sulfate. Then, filtration, evaporation, 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) ppm 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 번호US08134004B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-4169104e32c74b31b520149a50878912
출처 메모uspto-grants-2012_03