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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398024Generated: October 29, 2026

m-Chloroperbenzoic acid → Benzyl 6-oxa-3-azabicyclo(3.1.0)hexane-3-carboxylate

https://huagongshe.com/reaction/1398024

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantBenzyl 3-pyrroline-1-carboxylateHCID 643471—
SolventDichloromethaneHCID 6344—
ProductBenzyl 6-oxa-3-azabicyclo(3.1.0)hexane-3-carboxylateHCID 22147363—

Reaction Steps

To a stirred mixture of benzyl 2,5-dihydro-1H-pyrrole-1-carboxylate (5 g, 24.60 mmol) in DCM (80 mL) was added 3-chlorobenzoperoxoic acid (6.89 g, 30.75 mmol) at 0° C. The mixture was then stirred at rt overnight. The reaction mixture was then filtered through a bed of Celite and the filtrate was washed with sat'd aqueous Na2CO3 and brine. The organic was then separated and dried over anhydrous Na2SO4, filtered, and conc. in vacuo to yield the title compound that was used for next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901307B2
Source datasetuspto-grants-2014_12
ORD IDord-d7202e7f2796400293b4c7b0cdb5141a
Source noteuspto-grants-2014_12