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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888865Generated: October 26, 2026

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

https://huagongshe.com/reaction/1888865

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 numberUS08501774B2
Source datasetuspto-grants-2013_08
ORD IDord-91a0d73e52694516bf9e94d5b985f03c
Source noteuspto-grants-2013_08