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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193965Generated: October 27, 2026

Benzoyl Peroxide → 5-(Bromomethyl)-2-(trifluoromethyl)pyridine

https://huagongshe.com/reaction/1193965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant5-Methyl-2-(trifluoromethyl)pyridineHCID 14422791—
SolventCarbon TetrachlorideHCID 5943—
Product5-(Bromomethyl)-2-(trifluoromethyl)pyridineHCID 14405125—

Reaction Steps

5-Methyl-2-trifluoromethylpyridine (see J. Org. Chem., vol. 29, pages 569-571) (8.1 g) was dissolved in 50 ml of carbon tetrachloride, and N-bromosuccinimide (8.9 g) and a catalytic amount of benzoyl peroxide were added. The mixture was refluxed for 7 hours with stirring. The reaction mixture was cooled, and insoluble materials were collected by filtration. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography to give 2-trifluoromethyl-5-pyridylmethyl bromide (also known as 5-bromomethyl-2-trifluoromethylpyridine) (7.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04812454
Source datasetuspto-grants-1989_03
ORD IDord-91b60b8632604661b5679df154796bdd
Source noteuspto-grants-1989_03