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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173175Generated: October 31, 2026

1,4-Cyclohexanedione → 4-Hydroxy-4-phenylcyclohexan-1-one

https://huagongshe.com/reaction/1173175

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-CyclohexanedioneHCID 12511—
ReactantHCID 178418255HCID 178418255—
SolventTetrahydrofuranHCID 8028—
Product4-Hydroxy-4-phenylcyclohexan-1-oneHCID 58374122%

Reaction Steps

To a solution of 1,4-cyclohexanedione (6.72 g, 60 mmol) in THF (100 mL) cooled in an ice bath was added a 1 M solution of phenyl magnesium bromide in THF (20 mL, 20 mmol). The mixture was stirred at room temperature for 3 hours and quenched with an NH4Cl solution. The resulting solution was extracted with EtOAc three times. The combined organic phase was washed with brine, dried over MgSO4 and concentrated. Purification on silica gel eluting with 1:1 EtOAc/hexanes yielded 0.83 g (22%) of the title compound. MS calculated (M+H)+ 190, found 173 (M+H—H2O)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834021B2
Source datasetuspto-grants-2010_11
ORD IDord-5a1015c5a8e14142bdad1dbc26fa166f
Source noteuspto-grants-2010_11