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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767762Generated: November 1, 2026

m-Chloroperbenzoic acid → HCID 12094929, compound

https://huagongshe.com/reaction/1767762

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantEthyl 3-cyclopenten-1-ylbenzoateHCID 12094926—
SolventDichloromethaneHCID 6344—
ProductHCID 12094929HCID 12094929—

Reaction Conditions

Temperature0 °C

Reaction Steps

5 g (23 mmol) of ethyl 3-cyclopent-1-ylbenzoate (4a) and 100 ml of methylene chloride are introduced into a round-bottomed flask. The solution is cooled to 0° C. and 9 g (28 mmol) of meta-chloroperbenzoic acid are added in portions. The mixture is stirred for 30 minutes at 0° C. and then for 4 hours at room temperature. The mixture is filtered. The filtrate is successively washed with a saturated aqueous sodium thiosulfate solution, a saturated aqueous sodium bicarbonate solution and then with a saturated aqueous sodium chloride solution. The organic phase is dried over Na2SO4, filtered and concentrated under reduced pressure. The residue is purified by flash chromatography on silica gel (cyclohexane/ethyl acetate: 95:5). The title product is obtained in the form of a colorless oil (4.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235568B2
Source datasetuspto-grants-2007_06
ORD IDord-c5e91866ff564ecfb87353f6b6e11f99
Source noteuspto-grants-2007_06