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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539985Generated: October 31, 2026

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

https://huagongshe.com/reaction/539985

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 (2.5 g) in dichloromethane (60 mL) was added 3-chloroperoxybenzoic acid (6.08 g, 50-60% purity). The reaction was stirred at room temperature for 72 hours, and then a saturated sodium thiosulfate solution (50 mL) was added. After being stirred for additional 30 minutes, the mixture was extracted with chloroform (50 mL×2). The combined organic layers were washed successively with 2 N aqueous solution of sodium hydroxide (50 mL×2) and brine (50 mL), dried over magnesium sulfate and concentrated in vacuo to afford 2.79 g of the crude benzyl 6-oxa-3-azabicyclo[3.1.0]hexane-3-carboxylate as an oil. MS obsd. (ESI+) [(M+H)+] 220.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871756B2
Source datasetuspto-grants-2014_10
ORD IDord-9d002bb265c74eeb9a8f074bbc05fccb
Source noteuspto-grants-2014_10