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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263512Generated: November 1, 2026

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

https://huagongshe.com/reaction/1263512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridiniumHCID 4989215—
Reactant4-(1,4-Dioxaspiro[4.5]dec-8-yl)-1,3-benzenediolHCID 9921257—
SolventAcetoneHCID 180—
Product4-(2,4-Dihydroxyphenyl)cyclohexanoneHCID 9942489100%

Reaction Steps

A round bottomed flask was charged with 4-(1,4-dioxaspiro[4.5]dec8-yl)-1,3-benzenediol (11.3 g), acetone (250 ml) and water (50 ml). To the stirred solution was added pyridinium ptoluenesulfonate (1.14 g) 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 removing 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+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541473B2
Source datasetuspto-grants-2003_04
ORD IDord-b4c8b54733db46fbbf5359a0d1894487
Source noteuspto-grants-2003_04