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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1425939Generated: October 29, 2026

Benzoyl Peroxide → 1-Bromo-2-(bromomethyl)-3-(trifluoromethyl)benzene

https://huagongshe.com/reaction/1425939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant1-Bromo-2-methyl-3-(trifluoromethyl)benzeneHCID 2775634—
SolventCarbon TetrachlorideHCID 5943—
Product1-Bromo-2-(bromomethyl)-3-(trifluoromethyl)benzeneHCID 2275413699%

Reaction Steps

To a solution of 1-bromo-2-methyl-3-(trifluoromethyl)benzene (CXXVII) (5.7 g, 23.86 mmol) in CCl4 (50 mL) was added NBS (4.24 g, 23.86 mmol) and a catalytic amount of benzoyl peroxide. The reaction mixture was gently refluxed for 1 h. The reaction mixture was cooled to room temperature and the precipitate was removed by filtration. The solution was concentrated under reduced pressure and the crude product was dissolved in hexane and additional precipitate was removed by filtration. The filtrate was concentrated to dryness to give 1-bromo-2-(bromomethyl)-3-(trifluoromethyl)benzene (CXXVIII) as an orange oil (7.51 g, 23.62 mmol). 1H NMR (DMSO-d6) δ ppm 4.73 (s, 2H), 7.4 (dd, J=8 Hz, J=8 Hz, 1H), 7.80 (d, J=8 Hz, 1H), 8.02 (d, J=8 Hz, 1H); 19F NMR (DMSO-d6) δ ppm −57.85 (s, 3F). The crude product was used without further purification for step 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933018B2
Source datasetuspto-grants-2015_01
ORD IDord-0cdb4fbb43a047a7b58ce292db816977
Source noteuspto-grants-2015_01