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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6196생성일: 2026년 10월 23일

Hydrogen Bromide → 4,4'-(2,2,2-Trifluoro-1-phenylethane-1,1-diyl)diphenol

https://huagongshe.com/ko/reaction/6196

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen BromideHCID 260—
반응물AnisoleHCID 7519—
반응물2,2,2-TrifluoroacetophenoneHCID 9905—
반응물Trifluoromethanesulfonic acidHCID 62406—
용매Acetic AcidHCID 176—
생성물4,4'-(2,2,2-Trifluoro-1-phenylethane-1,1-diyl)diphenolHCID 19005175—

반응 단계

A mixture of 100 grams (0.57 mol) of trifluoroacetophenone, 100 grams (0.7 mol) trifluoromethane sulfonic acid, and 100 grams (10.9 mol) anisole is stirred at room temperature for 24 hours. The mixture is then transferred to a separatory funnel and the organic material is washed with water (3×11), saturated bicarbonate (3×500 ml) and water (2×500 ml). The organic phase is dried and the volatiles removed in vacuo. The resulting material is crystallized from aqueous methanol. 37.2 grams (0.1 mol) of this product is refluxed with glacial acetic acid saturated with anhydrous hydrobromic acid. The mixture is cooled and poured over crushed ice and the solid collected. The crude material is recrystallized from ethanol and petroleum ether to give 1,1-bis(4-hydroxyphenyl)-1-phenyl-2,2,2-trifluoroethane.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05247050
출처 데이터셋uspto-grants-1993_09
ORD IDord-7ba62443ec7649e18842d3f4e41dec27
출처 메모uspto-grants-1993_09