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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395856Generated: November 1, 2026

Cyclohexanone → Cyclohexanone, 2-(2-ethoxyethyl)-

https://huagongshe.com/reaction/2395856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
ReactantEthyl vinyl etherHCID 8023—
ReactantDi-tert-butyl peroxideHCID 8033—
ProductCyclohexanone, 2-(2-ethoxyethyl)-HCID 1101929795%

Reaction Steps

2940 g (30 mol) of cyclohexanone were heated to reflux while stirring and, at this temperature, a solution of 87.6 g (0.6 mol) of di-tert-butyl peroxide in 216 g (3 mol) of ethyl vinyl ether was added over the course of 5 hours (h). The mixture was subsequently refluxed for a further 1 h. After the mixture had cooled, the low boilers (tert-butanol, remaining vinyl ether and peroxide) and the excess cyclohexanone were removed by distillation under reduced pressure (25-40 mbar; diaphragm pump). The residue (about 500 g) was distilled under reduced pressure (0.5 to 2 mbar; oil pump). A total of 350 g of a 95% pure 2-(2-ethoxyethyl)cyclohexanone of boiling point 60°-65° C. (0.5 mbar) was obtained, corresponding to a yield of 69% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05489694
Source datasetuspto-grants-1996_02
ORD IDord-96ece210dd19420b8b8041f4b6f706f0
Source noteuspto-grants-1996_02