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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880787Generated: October 30, 2026

Phenyltrimethylammonium bromide dibromide → 2-Bromo-1-(3-chloro-5-(trifluoromethyl)pyridin-2-yl)ethanone

https://huagongshe.com/reaction/1880787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyltrimethylammonium bromide dibromideHCID 17977687—
Reactant1-(3-Chloro-5-trifluoromethyl-pyridin-2-yl)-ethanoneHCID 21712136—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-1-(3-chloro-5-(trifluoromethyl)pyridin-2-yl)ethanoneHCID 86057596—

Reaction Steps

To a solution of 16.6 g (0.074 mol) of 1-[3-chloro-5-(trifluoromethyl)-2-pyridinyl]ethanone in 150 ml of dry tetrahydrofuran, were added portionwise at room temperature 27.8 g (0.074 mol) of phenyltrimethylammonium tribromide. The solution was stirred for 3 hours at room temperature. The formed solid was removed by filtration and the mother liquors were concentrated under vacuum. The resulting orange oil (32.7 g) was purified by flash chromatography on silica gel (eluent: heptane/dichloromethane 3:1) to give 2-bromo-1-[3-chloro-5-(trifluoromethyl)-2-pyridinyl]ethanone: 10.4 g (46%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318777B2
Source datasetuspto-grants-2012_11
ORD IDord-b560b56f6c3241cc88b714dbc15b3c39
Source noteuspto-grants-2012_11