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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363554Generated: October 27, 2026

Cyclohexanone → 1-Allyl-1-cyclohexanol

https://huagongshe.com/reaction/1363554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
ReactantHCID 178455850HCID 178455850—
SolventDiethyl EtherHCID 3283—
Product1-Allyl-1-cyclohexanolHCID 79145—

Reaction Steps

A solution of allyl magnesium bromide in diethyl ether (1 M, 53 mL, 53 mmol) was added dropwise to a solution of cyclohexanone (5.00 mL, 48.2 mmol) in diethyl ether at 0° C. The cloudy white reaction mixture was allowed to stir at rt overnight. The reaction was quenched with saturated aqueous NH4Cl (100 mL) and diluted with water (20 mL) and diethyl ether (50 mL). The mixture was transferred to a separatory funnel and the layers were separated. The aqueous layer was extracted with diethyl ether (2×50 mL). The combined organic layers were washed with brine (100 mL), dried over MgSO4, filtered, and concentrated to afford a 1-allylcyclohexanol as a colorless oil (6.97, 103%) that contained a small amount of diethyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884207B2
Source datasetuspto-grants-2011_02
ORD IDord-7178fce3be0e41d1b5429b85f49bc450
Source noteuspto-grants-2011_02