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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1669642생성일: 2026년 10월 26일

Phenol → 4,4'-[4-(Trifluoromethyl)cyclohexane-1,1-diyl]diphenol

https://huagongshe.com/reaction/1669642

반응식

참여 물질

역할이름HCID투입량
반응물PhenolHCID 996—
반응물4-(Trifluoromethyl)cyclohexanoneHCID 2777491—
용매Hydrochloric AcidHCID 313—
용매Ethyl AcetateHCID 8857—
용매Sodium BicarbonateHCID 516892—
생성물4,4'-[4-(Trifluoromethyl)cyclohexane-1,1-diyl]diphenolHCID 67333442—

반응 단계

A solution of 4-(trifluoromethyl)cyclohexanone (1.13 g, 6.8 mmol) and phenol (2.01 g, 21.4 mmol) in 3 mL of concentrated HCl (aq) was stirred at 40° C. for 18 h. The reaction mixture was diluted with EtOAc and saturated aqueous NaHCO3 was slowly added. The organic layer was collected and the aqueous layer was extracted twice with EtOAc. The combined organic layers were concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with a gradient of 0% to 40% EtOAc/hexanes over 10 column volumes, then 40% to 100% EtOAc/hexanes over 5 column volumes, affording the title compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07989472B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-66dcd8f751764dc8aef01be8a59c9e70
출처 메모uspto-grants-2011_08