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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041332Generated: November 2, 2026

Benzoyl Peroxide → HCID 57655944, compound

https://huagongshe.com/reaction/2041332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 57656139HCID 57656139—
SolventWaterHCID 962—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 57655944HCID 5765594455%

Reaction Steps

To 1-methyl-4-(3,3,3-trifluoro-2-methyl-2-trifluoromethylpropane-1-sulfinyl)-benzene (4.13 g, 13.0 mmol) in carbon tetrachloride (50 mL) add NBS (2.31 g, 13.0 mmol), benzoyl peroxide (314 mg, 1.30 mmol) and stir overnight at reflux. Cool to ambient temperature, dilute with water and extract three times with EtOAc. Dry over anhydrous Na2SO4 and concentrate in vacuo. Purify by chromatography on silica gel eluting with hexane/EtOAc (9:1) to give the title compound as colorless oil (2.3 g, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580780B2
Source datasetuspto-grants-2013_11
ORD IDord-fa9f341384cf463ea06cdab414383daf
Source noteuspto-grants-2013_11