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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717538Generated: November 1, 2026

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

https://huagongshe.com/reaction/1717538

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 C9H15NO3: 185.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803839B2
Source datasetuspto-grants-2010_09
ORD IDord-97d4de66133d4c909008b46623d65305
Source noteuspto-grants-2010_09