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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274832Generated: October 30, 2026

Sodium Cyanide → 2-(2,3,5-Trichlorophenyl)acetonitrile

https://huagongshe.com/reaction/274832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
Reactant1-(Bromomethyl)-2,3,5-trichlorobenzeneHCID 19705045—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-(2,3,5-Trichlorophenyl)acetonitrileHCID 1970509970%

Reaction Conditions

Temperature35 °C

Reaction Steps

A solution of 19.2 grams (0.070 mole) of 2,3,5-trichlorophenylmethyl bromide in 50 mL of methanol was stirred, and a solution of 4.1 grams (0.084 mole) of sodium cyanide in 10 mL of water was added dropwise during a 10 minute period. The addition caused an exothermic reaction which raised the reaction mixture temperature to about 35° C. Upon completion of addition, the reaction mixture was warmed to reflux, where it was stirred for 4.5 hours. The reaction mixture was allowed to cool to ambient temperature, where it was stirred for about 60 hours. After this time the reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The extract was washed with two portions of water, two 25 mL portions of aqueous 10% hydrochloric acid, and then with three portions of water. The organic layer was dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure, yielding 10.8 grams of 2,3,5-trichlorophenylacetonitrile. The infrared spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05391541
Source datasetuspto-grants-1995_02
ORD IDord-bc2635b3d5b54736a7e27d5ccb050329
Source noteuspto-grants-1995_02