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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370325Generated: October 31, 2026

m-Chloroperbenzoic acid → (+/-)-7-(2'-Acetoxyethyl)-2-oxepanone

https://huagongshe.com/reaction/370325

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(2'-Acetoxyethyl) cyclohexanoneHCID 11126942—
SolventDichloromethaneHCID 6344—
Product(+/-)-7-(2'-Acetoxyethyl)-2-oxepanoneHCID 23283899—

Reaction Steps

Under an argon atmosphere, sodium bicarbonate (1.78 g, 21.20 mmol) and 80-90% w/w MCPBA (4.95 g, 28.26 mmol) were added to a solution of (±)-2-(2'-acetoxyethyl)cyclohexanone (2.60 g, 14.13 mmol) (0.50 mmol) in dichloromethane (70 ml) at room temperature. The mixture was stirred at room temperature for 3 h, and diluted with dichloromethane (80 ml) and washed sequentially with a saturated sodium sulphite solution (3×100 ml), distilled water (100 ml) and brine (100 ml). The organic phase was dried over magnesium sulphate. After filtration, the solvent was evaporated under reduced pressure to give the crude product which was purified by flash column chromatography using hexane-ethyl acetate (2:3) as eluent to give (±)-7-(2'-acetoxyethyl)-2-oxepanone, as a colourless oil (2.76 g, 98% yield). Rf 0.40 (hexane-ethyl acetate, 7:3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140512
Source datasetuspto-grants-2000_10
ORD IDord-a22791c55d7144289f59ea0e3740ed9c
Source noteuspto-grants-2000_10