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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015962Generated: October 27, 2026

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

https://huagongshe.com/reaction/1015962

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 numberUS07985730B2
Source datasetuspto-grants-2011_07
ORD IDord-1dedf848b0004789b8dea46dcb00dd46
Source noteuspto-grants-2011_07