Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922016Generated: October 28, 2026

Water → 4-(bromomethyl)-3-(trifluoromethyl)benzonitrile

https://huagongshe.com/reaction/1922016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant4-Methyl-3-(trifluoromethyl)benzonitrileHCID 2775598—
SolventCarbon TetrachlorideHCID 5943—
Product4-(bromomethyl)-3-(trifluoromethyl)benzonitrileHCID 5882716098.1%

Reaction Steps

4-methyl-3-(trifluoromethyl)benzonitrile (10 g, 54 mmol) was dissolved in 200 mL of carbon tetrachloride and treated with N-bromosuccinimide (10.5 g, 59 mmol) and benzoyl peroxide (1.3 g, 0.54 mmol). The reaction mixture was heated to reflux temperature and stirred for one week. Then, 80 mL of water was added and the layers were separated. The aqueous layer was extracted with methylene chloride (2×50 mL). The combined organic layers were washed with water (2×50 mL), dried over magnesium sulfate, and concentrated to provide 4-(bromomethyl)-3-(trifluoromethyl)benzonitrile (14 g, 53 mmol) as a yellow oil which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173805B2
Source datasetuspto-grants-2012_05
ORD IDord-ec72eb13e95c470ba210fd4edaf5b626
Source noteuspto-grants-2012_05