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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929757Generated: October 31, 2026

Sodium Thiosulfate → Benzyl 6-oxa-3-azabicyclo(3.1.0)hexane-3-carboxylate

https://huagongshe.com/reaction/1929757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantBenzyl 3-pyrroline-1-carboxylateHCID 643471—
SolventDichloromethaneHCID 6344—
ProductBenzyl 6-oxa-3-azabicyclo(3.1.0)hexane-3-carboxylateHCID 22147363103.5%

Reaction Steps

To a solution of 1-benzyloxycarbonyl-3-pyrroline (5.0 g) in methylene chloride (125 mL) was added m-chloroperbezoic acid (12.17 g) and the mixture was stirred at room temperature for 3 days. To the reaction mixture was added an aqueous saturated sodium thiosulfate solution (100 mL) and the mixture was stirred for 30 minutes. The reaction mixture was extracted with chloroform (×2) and the organic layer was washed successively with an aqueous 2N sodium hydroxide solution (1100 mL×2) and a saturated brine, dried over magnesium sulfate and concentrated in vacuo to give benzyl 6-oxa-3-azabicyclo[3,1,0]hexan-3-carboxylate (5.58 g, yield: 100%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188097B2
Source datasetuspto-grants-2012_05
ORD IDord-b2c2feab50544c8b830be3b9dbf79fc8
Source noteuspto-grants-2012_05