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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165839Generated: October 29, 2026

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

https://huagongshe.com/reaction/1165839

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 at α-(4-chlorophenyl)-2-methoxy-4-nitrobenzeneacetonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04912106
Source datasetuspto-grants-1990_03
ORD IDord-1325d139c5a84b63a55fe1eb14766557
Source noteuspto-grants-1990_03