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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911452Generated: October 30, 2026

Benzoyl Peroxide → HCID 57655944, compound

https://huagongshe.com/reaction/911452

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 numberUS08022062B2
Source datasetuspto-grants-2011_09
ORD IDord-9dc09865dcfd493b81e70c351c4ea2d9
Source noteuspto-grants-2011_09