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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710025Generated: November 1, 2026

Hydrochloric Acid → alpha-(4-Chlorophenyl)-2-methoxy-4-nitrobenzeneacetonitrile

https://huagongshe.com/reaction/1710025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant2-Chloro-5-nitroanisoleHCID 70519—
Reactant4-Chlorobenzyl cyanideHCID 241582—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventTetrahydrofuranHCID 8028—
Productalpha-(4-Chlorophenyl)-2-methoxy-4-nitrobenzeneacetonitrileHCID 23035215—

Reaction Steps

To a stirred mixture of 68 parts of 1-chloro-2-methoxy-4-nitrobenzene, 230 parts of a sodium hydroxide solution 50%, 5 parts of N,N,N-triethylbenzenemethanaminium chloride and 360 parts of tetrahydrofuran is added dropwise, during a 5 minutes period, a solution of 43.2 parts of 4-chlorobenzeneacetonitrile in 90 parts of tetrahydrofuran. Upon completion, stirring is continued for 4 hours at 60° C. The reaction mixture is poured into 2000 parts of crushed ice. The whole is acidified with concentrated hydrochloric acid. The layers are separated. The aqueous phase is extracted with dichloromethane. The combined extracts are dried, filtered and evaporated. The residue is crystallized from 2,2'-oxybispropane. The product is filtered off and dried, yielding α-(4-chlorophenyl)-2-methoxy-4-nitrobenzeneacetonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04952570
Source datasetuspto-grants-1990_08
ORD IDord-3856380e30dd47a78573e90610047523
Source noteuspto-grants-1990_08