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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387222Generated: October 25, 2026

Potassium Cyanide → (4-Bromo-2-chlorophenyl)acetonitrile

https://huagongshe.com/reaction/387222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
Reactant4-Bromo-1-(bromomethyl)-2-chlorobenzeneHCID 21914486—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventWaterHCID 962—
Solvent1,1-DichloroethaneHCID 6365—
Product(4-Bromo-2-chlorophenyl)acetonitrileHCID 58762522290.2%

Reaction Steps

To a stirred solution of 4-bromo-1-bromomethyl-2-chlorobenzene (16, 62.5 g, 0.22 mol) in dichloroethane (522 mL) and water (480 mL) was added tetrabutylammonium chloride (5.05 g), followed by a solution of potassium cyanide (43.2 g, 75.8 mmol) in water (523 mL). and the solution was stirred for 4 h at room temperature. The layers were separated and the aqueous layer was extracted with dichloroethane (100 mL). The combined organic layers were washed with water (100 mL), dried over sodium sulfate filtered and evaporated. The crude product (52 g) was distilled under reduced pressure (1 mmHg), affording (4-bromo-2-chlorophenyl)-acetonitrile (45.5 g, 0.220 mol, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372970B2
Source datasetuspto-grants-2013_02
ORD IDord-ad2cc4d86cd74f9d935f696782859fe3
Source noteuspto-grants-2013_02