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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354089Generated: October 31, 2026

2-Chlorocyclohexanone → 2-(4-Chlorophenyl)cyclohexan-1-one

https://huagongshe.com/reaction/1354089

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorocyclohexanoneHCID 13203—
ReactantHCID 178478191HCID 178478191—
SolventDiethyl EtherHCID 3283—
Product2-(4-Chlorophenyl)cyclohexan-1-oneHCID 383956673.8%

Reaction Steps

A solution of 4-chlorophenylmagnesium bromide (200 mL of 1 M in ether, 200 mmol) was cooled in an ice-bath and a solution of 2-chlorocyclohexanone (26.5 g, 200 mmol) in 200 mL of ether was slowly added. The mixture was stirred at room temperature for 4 hours and was then concentrated under reduced pressure. Benzene (300 mL) was added and the mixture was heated under reflux for 12 h. Dilute aqueous HCl was added and the organic layer was separated, washed with brine, dried (sodium sulfate) and evaporated. Bulb-to-bulb distillation (2 mm) afforded 30.8 g of liquid product that subsequently crystallized.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223767B2
Source datasetuspto-grants-2007_05
ORD IDord-a614873a65dd4c50b079bde0cf9bd5d0
Source noteuspto-grants-2007_05