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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977637Generated: October 31, 2026

m-Chloroperbenzoic acid → HCID 11121760, compound

https://huagongshe.com/reaction/977637

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 11089029HCID 11089029—
SolventDichloromethaneHCID 6344—
ProductHCID 11121760HCID 1112176090.7%

Reaction Steps

1.5 g of 3-chloroperoxybenzoic acid was added, whilst ice-cooling, to a solution of 2 g of (3S,4R)-3-[(1R)-1-t-butyldimethylsilyloxyethyl]-4-phenylthio-2-azetidinone [prepared as described in step (i) above] in 30 ml of methylene chloride, and the resulting mixture was stirred at room temperature for 6 hours. At the end of this time, the reaction mixture was mixed with 30 ml of methylene chloride, and the organic layer was separated and washed with water, with a saturated aqueous solution of sodium hydrogencarbonate and again with water, in that order. It was then dried over anhydrous magnesium sulfate, and the solvent was removed by distillation under reduced pressure. The resulting residue was purified by flash chromatography, using a 1:1 by volume mixture of cyclohexane and ethyl acetate as the eluent, to give 1.9 g of the title compound consisting of two diastereomers, differing in the configuration of the sulfoxide group, as colorless crystals, melting at 65°-70° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05614624
Source datasetuspto-grants-1997_03
ORD IDord-2719ec3a481542c1bb8c38607456d478
Source noteuspto-grants-1997_03