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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279669Generated: October 26, 2026

m-Chloroperbenzoic acid → Benzyl 1-oxa-5-azaspiro[2.4]heptane-5-carboxylate

https://huagongshe.com/reaction/2279669

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
Reactant1-Cbz-3-methylenepyrrolidineHCID 18412247—
SolventDichloromethaneHCID 6344—
SolventSodium SulfiteHCID 24437—
ProductBenzyl 1-oxa-5-azaspiro[2.4]heptane-5-carboxylateHCID 71649494—

Reaction Steps

A solution 3-methylen-pyrrolidine-1-carboxylic acid benzyl ester (WO9624593) in 5 ml of dichloromethane was treated with 2.16 g sodium bicarbonate (MW: 84.01 26.28 mmol) and 2.47 g of 80% m-chlor-perbenzoic acid (MW: 172.57, 11.48 mmol). The reaction mixture was stirred at room temperature for three hours. The reaction mixture was diluted with 20 ml of a saturated aqueous sodium sulfite solution and 45 ml of dichloromethane. The organic layer was successively washed with 30 ml of an aqueous saturated sodium bicarbonate solution and brine. The organic layer was dried over magnesium sulfate. The residue was purified by chromatography on silica (1/1 ethyl acetate/n-hexane) to afford a off white solid. Yield: 440 mg, 57%. MS: 234.1 (M+H)+, Method ESI+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133213B2
Source datasetuspto-grants-2015_09
ORD IDord-c3ab11fabdc54c6aae863fa9e6374b4b
Source noteuspto-grants-2015_09