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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847136Generated: October 29, 2026

m-Chloroperbenzoic acid → HCID 178527108, compound

https://huagongshe.com/reaction/847136

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 9992727HCID 9992727—
SolventChloroformHCID 6212—
ProductHCID 178527108HCID 17852710870.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-(2-phenylethyl)-1,3,2-benzodithiazole (0.538 g, 2.08 mmol), from Step 2, in 30 mL of chloroform at -20° C., was added portionwise 56% meta-chloroperoxybenzoic acid (mCPBA) (0.64 g, 2 mmol). The reaction mixture was allowed to warm to 0° C. over a 2 hour period and then the reaction was quenched at 10° C. with 20 mL of 1M aqueous sodium bicarbonate solution. The organic layer was concentrated in vacuo and the residue was purified by column chromatography on silica gel eluting with chloroform (CHCl3) to give 389 mg (65.7% yield) of the title compound. Analysis calculated for C14H13NOS2 : C, 61.08; H, 4.76; N, 5.09. Found: C, 60.92; H, 4.75; N, 5.04.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05140018
Source datasetuspto-grants-1992_08
ORD IDord-9f256fac248842bcb15ca02d9f54862b
Source noteuspto-grants-1992_08