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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 346818생성일: 2026년 10월 26일

Water → 4-(2,4-Dihydroxyphenyl)cyclohexanone

https://huagongshe.com/reaction/346818

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
반응물4-(1,4-Dioxaspiro[4.5]dec-8-yl)-1,3-benzenediolHCID 9921257—
용매AcetoneHCID 180—
생성물4-(2,4-Dihydroxyphenyl)cyclohexanoneHCID 9942489100%

반응 단계

A flask equipped with magnetic stirrer was charged with 4-(1,4-dioxaspiro[4.5]dec-8-yl)-1,3-benzenediol (11.3 g, 45.2 mmol), acetone (250 ml) and water (50 ml). To the stirred solution was added pyridinium p-toluenesulfonate (1.14 g, e.52 mmol) in one portion and the reaction mixture as then heated under reflux for 8 hr. After allowing the reaction mixture to cool to room temperature, most of the acetone was removed in vacuo and the remaining mixture was partitioned between ethyl acetate (200 ml) and water (50 ml). The aqueous layer extracted with ethyl acetate (3 ×50 ml) and the combined organic layers were washed with brine (30 ml), dried (MgSO4), filtered and concentrated under reduced pressure to afford an off-white powder. After washing the powder with dichloromethane (100 ml) and removal of excess solvent under reduced pressure, the title compound (9.30 g, 100%) was obtained as an off-white powder. M/z (ES+) 207 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07173052B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-99894fcc20fa47169198ab69853e9e3a
출처 메모uspto-grants-2007_02