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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203706Generated: October 27, 2026

Diethyl Ether → Benzyl 7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate

https://huagongshe.com/reaction/2203706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant1,2,3,6-Tetrahydropyridine-1-carboxylateHCID 21691317—
SolventDichloromethaneHCID 6344—
ProductBenzyl 7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylateHCID 1318688899%

Reaction Steps

3-Chlorobenzoperoxoic acid (51.1 g, 228 mmol) was added portion wise to a solution of 5,6-dihydropyridine-1(2H)-carboxylate (33.0 g, 152 mmol) in DCM (200 mL) at 0° C. After 10 minutes at 0° C., the reaction was warmed to room temperature and stirred at room temperature for 4 hours. The reaction mixture was diluted with ether (800 mL), washed with 1N NaOH solution (2×200 mL), saturated N2SO3 solution (2×100 mL), brine (100 mL), dried (sodium sulfate) and concentrated in vacuo to give benzyl 7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate (35.0 g, 99%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365568B2
Source datasetuspto-grants-2016_06
ORD IDord-ddb00c2aafcb4a20b5f8e3a19a54133f
Source noteuspto-grants-2016_06