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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387087Generated: November 3, 2026

Potassium Cyanide → 2-[4-Bromo-2-(trifluoromethyl)phenyl]acetonitrile

https://huagongshe.com/reaction/2387087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
Reactant4-Bromo-1-(bromomethyl)-2-(trifluoromethyl)benzeneHCID 53418031—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWater methylene chlorideHCID 21908982—
Product2-[4-Bromo-2-(trifluoromethyl)phenyl]acetonitrileHCID 5848840754.1%

Reaction Steps

A mixture of 4-methyl-3-trifluorobromobenzene (33.26 g, 104.261 mmol) from step 1 above, KCN (20.43 g, 313.67 mmol) and tetrabutylammonium bromide (3.37 g, 10.45 mmol) in CH2Cl2/H2O 1:1 (300 mL) was stirred at room temperature for 4 hours. The layers were separated and the organic layer washed with H2O (100 mL) 1N HCl (100 mL), brine, dried over Na2SO4 and then concentrated to a brown oil which was purified by flash column chromatography (0% to 20% EtOAc in hexanes) to give the product as a clear oil (14.9 g, 54%). 1H NMR (400 MHz, CDCl3) δ 3.91 (s, 2H), 7.57 (d, J=8.3 Hz, 1 H), 7.75 (dd, J=8.3, 2 Hz, 1 H), 7.84 (d, J=2 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268835B2
Source datasetuspto-grants-2012_09
ORD IDord-f5469e9e8cfd458fa9611b5a2949ea07
Source noteuspto-grants-2012_09