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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341674Generated: October 27, 2026

m-Chloroperbenzoic acid → 4-(4-Bromo-2-ethylphenyl)-2,2,6,6-tetramethyl-1-oxo-dihydrothiopyran-3,5-dione

https://huagongshe.com/reaction/341674

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant4-(4-Bromo-2-ethylphenyl)-2,2,6,6-tetramethylthiopyran-3,5-dioneHCID 68733026—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-(4-Bromo-2-ethylphenyl)-2,2,6,6-tetramethyl-1-oxo-dihydrothiopyran-3,5-dioneHCID 6873367954.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 3-chloroperbenzoic acid (2.45 g, 0.0142 mol) in dichloromethane (40 ml) is added to a pre-cooled solution (0° C.) of 4-(4-bromo-2-ethylphenyl)-2,2,6,6-tetramethyl-thiopyran-3,5-dione (3.5 g, 0.0095 mol) in dichloromethane (100 ml). The reaction mixture is stirred at 0° C. for one hour and then allowed to come to room temperature. The reaction mixture is stirred at room temperature for one hour, diluted with water (100 ml) and separated. The organic phase is collected, and the aqueous layer is extracted with dichloromethane (2×50 ml). The organic phases are combined, washed with water, and dried over anhydrous sodium sulfate. The mixture is filtered, and the filtrate is evaporated under reduced pressure. The residue is purified by column chromatography on silica gel to give 4-(4-bromo-2-ethylphenyl)-2,2,6,6-tetramethyl-1-oxo-dihydrothiopyran-3,5-dione as a white solid (2.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895761B2
Source datasetuspto-grants-2014_11
ORD IDord-82da870b120643d081476f32c88360b2
Source noteuspto-grants-2014_11