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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1188053Generated: November 1, 2026

m-Chloroperbenzoic acid → 5-Fluoro-2-(methylsulfinyl)benzo[d]thiazole

https://huagongshe.com/reaction/1188053

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant5-Fluoro-2-(methylthio)benzo[d]thiazoleHCID 55252707—
SolventDichloromethaneHCID 6344—
Product5-Fluoro-2-(methylsulfinyl)benzo[d]thiazoleHCID 5818062694%

Reaction Steps

5-Fluoro-2-(methylthio)benzo[d]thiazole (example 40A, 0.178 g, 0.893 mmol) was dissolved in CH2Cl2 (5.96 mL). mCPBA (0.154 g, 0.893 mmol) was added in one portion and the reaction mixture was stirred at room temperature. The reaction was quenched with saturated aqueous sodium bicarbonate and diluted with dichloromethane. The aqueous layer was extracted with dichloromethane (2×). The combined organic were washed with brine, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. 5-Fluoro-2-(methylsulfinyl)benzo[d]thiazole (0.180 g, 94% yield) was isolated as a white solid and used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673933B2
Source datasetuspto-grants-2014_03
ORD IDord-b4accc5624d14c4485897e7f3236bef6
Source noteuspto-grants-2014_03