돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 585686생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/585686

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 round bottomed 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, 4.52 mmol) in one portion and the reaction mixture was then heated to reflux temperature 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 was extracted with ethyl acetate (3×50 ml) and the combined organic layers were washed with brine (30 ml), dried over magnesium sulfate, 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 desired product (9.30 g, 100%) was obtained as an off-white white powder. m/z (ES+) 207 (M+H+); δH(CD3OD) 1.84-1.97 (2H, m), 2.15-2.23 (2H, m), 2.36-2.45 (2H, m), 2.58-2.68 (2H, m), 3.39 (1H, tt), 6.26 (1H, dd), 6.34 (1H, d), 6.96 (1H, d).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06933319B2
출처 데이터셋uspto-grants-2005_08
ORD IDord-8f4b9153cc9a412eb41a59f49848f925
출처 메모uspto-grants-2005_08