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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544813Generated: October 28, 2026

Benzoyl chloride → HCID 67201259, compound

https://huagongshe.com/reaction/544813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantCyclohexane ethylacetateHCID 21867204—
Reactant1-(2-Hydroxy-5,5-dimethylcyclohexyl)pent-4-en-1-oneHCID 67201493—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 67201259HCID 6720125928.4%

Reaction Conditions

Temperature45 °C

Reaction Steps

Benzoyl chloride (12.8 g, 91 mmoles) was added dropwise to a stirred solution of 1-(2-hydroxy-5,5-dimethyl-1-cyclohexyl)-4-penten-1-one (16 g, 75 mmoles), Et3N (10 g, 99 mmoles) and DMAP (1.8 g, 15 mmoles) in CH2Cl2 (380 ml) at 20° C. and under nitrogen. The solution was heated at 45° C. during 22 hours, cooled to room temperature and washed successively with 5% aqueous HCl, 10% aqueous Na2CO3, and again with water. The organic phase was dried over Na2SO4 and concentrated to afford a brown oil. Chromatography (SiO2, AcOEt/Cyclohexane 1:9) and afforded 6.7 g of the title compound (yield=28%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935669B2
Source datasetuspto-grants-2011_05
ORD IDord-b23b071b319f4df2a067183d468ea3a9
Source noteuspto-grants-2011_05