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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499466Generated: November 1, 2026

m-Chloroperbenzoic acid → Benzyl 7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate

https://huagongshe.com/reaction/1499466

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantBenzyl 5,6-dihydropyridine-1(2H)-carboxylateHCID 11458613—
SolventDichloromethaneHCID 6344—
ProductBenzyl 7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylateHCID 13186888—

Reaction Steps

mCPBA (14.6 g, 63.3 mmol) was added slowly to a stirred solution of benzyl 3,6-dihydropyridine-1(2H)-carboxylate (12.50 g, 57.5 mmol) in DCM (80 mL) which was cooled in an ice bath. The reaction mixture was allowed to warm to room temperature and stirred for 16 h. The reaction mixture was then quenched with aq. Na2CO3 and the organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure to give the sub-title compound. LCMS calc. for C13H16NO3 (M+H)+: m/z=234.1. Found: 234.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09200004B2
Source datasetuspto-grants-2015_12
ORD IDord-daeb57a57e564901a17516b7756ea4f6
Source noteuspto-grants-2015_12