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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808942Generated: November 3, 2026

m-Chloroperbenzoic acid → Tert-butyl 1-oxa-5-azaspiro[2.3]hexane-5-carboxylate

https://huagongshe.com/reaction/1808942

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactanttert-Butyl 3-methylideneazetidine-1-carboxylateHCID 55269097—
SolventChloroformHCID 6212—
ProductTert-butyl 1-oxa-5-azaspiro[2.3]hexane-5-carboxylateHCID 6652177051%

Reaction Steps

To a solution of 1,1-dimethylethyl 3-methylideneazetidine-1-carboxylate (2.96 g, 17.5 mmol) in chloroform (180 mL) was added 3-chloroperoxybenzoic acid (77%, 13.9 g, 62.0 mmol), and the resulting mixture was stirred at room temperature for 2 days. The reaction mixture was quenched with a 1:1 mixture (150 mL) of 10% sodium thiosulfate and saturated sodium bicarbonate solutions. The organic portion was isolated, dried over sodium sulfate, filtered and concentrated to give an oily residue which was then purified by flash chromatography (15-50% ethyl acetate-hexanes) to give 1,1-dimethylethyl 1-oxa-5-azaspiro[2.3]hexane-5-carboxylate (1.65 g, 51%), GC-MS for C9H5NO3: 185.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362002B2
Source datasetuspto-grants-2013_01
ORD IDord-643b9f238c514c28bdee2b9f67f0e72f
Source noteuspto-grants-2013_01