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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850367Generated: October 29, 2026

m-Chloroperbenzoic acid → HCID 70287772, compound

https://huagongshe.com/reaction/850367

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantZ-321HCID 9798234—
SolventChloroformHCID 6212—
ProductHCID 70287772HCID 7028777273%

Reaction Steps

Dissolved in 100 ml of chloroform were 5 g of 3-(2-indanacetyl)-4(R)-(1-pyrrolidinecarbonyl)thiazolidine (a compound according to Preparation Example 2 set forth in Japanese Patent Application Laid-Open No. 262557/1990). While chilling with ice water, 3.3 g of meta-chloro-perbenzoic acid were gradually added to the solution. After stirring the mixture for 3 hours, the resultant liquid reaction mixture was washed successively with a 5% solution of sodium thiosulfate and a saturated aqueous solution of sodium bicarbonate and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by column chromatography on silica gel (methanol:chloroform=5:95), thereby obtaining 3.8 g of the title compound as a diastereomeric mixture. Yield: 73%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06017929
Source datasetuspto-grants-2000_01
ORD IDord-dc38d8cd4eb146cca81276f4c7bc9ba8
Source noteuspto-grants-2000_01