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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385008Generated: October 31, 2026

m-Chloroperbenzoic acid → 3-(3,5-Dichloro-4-methoxybenzoyl)-1-oxo-2,3-dihydro-1,3-benzothiazole

https://huagongshe.com/reaction/385008

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantBenzo[d]thiazol-3(2H)-yl(3,5-dichloro-4-methoxyphenyl)methanoneHCID 68109358—
SolventChloroformHCID 6212—
Product3-(3,5-Dichloro-4-methoxybenzoyl)-1-oxo-2,3-dihydro-1,3-benzothiazoleHCID 6810833664.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-(3,5-dichloro-4-methoxybenzoyl)-2,3-dihydro-1,3-benzothiazole (500 mg) was dissolved in chloroform (10 mL), and 70% metachloroperbenzoic acid (320 mg) was added to the solution, and the mixture was stirred at 0° C. for 10 minutes. The solvent was distilled off under reduced pressure and water was added, and then the mixture was extracted with ethyl acetate. The organic layer was washed with 1N sodium hydroxide and saturated brine, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:1) to obtain the title compound (336 mg) as a colorless crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367843B2
Source datasetuspto-grants-2013_02
ORD IDord-2e437cf7552243edb82282d402d56e02
Source noteuspto-grants-2013_02