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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 639523Generated: November 2, 2026

Sodium Cyanide → 2-(4-Chloro-3-trifluoromethyl-phenyl)-ethylamine hydrochloride

https://huagongshe.com/reaction/639523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
Reactant4-Chloro-3-(trifluoromethyl)benzyl bromideHCID 2778114—
Reactant2-(4-Chloro-3-(trifluoromethyl)phenyl)acetonitrileHCID 5004685—
SolventDimethyl SulfoxideHCID 679—
Product2-(4-Chloro-3-trifluoromethyl-phenyl)-ethylamine hydrochlorideHCID 68560752—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 4-bromomethyl-1-chloro-2-trifluoromethyl-benzene (3.94 g, 14.4 mmol) and sodium cyanide (1.06 g, 21.6 mmol) in dimethyl sulfoxide (12 mL) was heated at 50° C. for one hour. The reaction mixture was then poured on ice water and extracted four times with dichloromethane. The combined organic phases were washed with water, dried over magnesium sulfate, filtered and concentrated, leading to (4-chloro-3-trifluoromethyl-phenyl)-acetonitrile (3.19 g, 14.4 mmol) as a dark red oil. This crude material was transformed into the title compound in accordance with the general method of example H2. White solid, MS (ISP) 224.1 (M−Cl)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691876B2
Source datasetuspto-grants-2010_04
ORD IDord-54f84f45b84d4484bbd2c61b7056c7d3
Source noteuspto-grants-2010_04