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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358881Generated: October 26, 2026

Water → tert-Butyl 6-Oxa-3-azabicyclo(3.1.0)hexane-3-carboxylate

https://huagongshe.com/reaction/358881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactanttert-Butyl 2,5-dihydro-1H-pyrrole-1-carboxylateHCID 5148195—
SolventChloroformHCID 6212—
Producttert-Butyl 6-Oxa-3-azabicyclo(3.1.0)hexane-3-carboxylateHCID 1010388058.8%

Reaction Steps

2.96 g (0.012 mole) of 70% aqueous m-chloroperbenzoic acid were added to a solution of 1.69 g (0.01 mole) of 1-t-butoxycarbonyl-3-pyrroline [prepared as described in Step (a) above] in 10 ml of chloroform, whilst ice-cooling, and the mixture was stirred with ice-cooling for 8 hours and then with water-cooling for 15 hours. At the end of this time, the reaction mixture was extracted with toluene and the extract was washed, in turn, with an aqueous solution of sodium bicarbonate, a 0.1N aqueous solution of sodium thiosulfate and water. It was then dried over anhydrous sodium sulfate, and the solvent was removed by evaporation under reduced pressure. The residue was subjected to silica gel column chromatography eluted with a 1:5 by volume mixture of ethyl acetate and toluene, to afford 1.09 g of 1-t-butoxycarbonyl-3,4-epoxypyrrolidine as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04997943
Source datasetuspto-grants-1991_03
ORD IDord-3b5843a477ee452f954ed9e0b498034d
Source noteuspto-grants-1991_03