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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389936Generated: October 31, 2026

Chloroform → HCID 20296005, compound

https://huagongshe.com/reaction/1389936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantPotassium CyanideHCID 9032—
ReactantHCID 20296029HCID 20296029—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventWaterHCID 962—
ProductHCID 20296005HCID 20296005—

Reaction Steps

To a stirred solution of 7.45 parts of N-[chloro(2,6-dichlorophenyl)methylene]-2-methylbenzenamine in 150 parts of trichloromethane is added a solution of 4.88 parts of potassium cyanide and 8.5 parts of N,N,N-triethylbenzenemethanaminium chloride in 8 parts of water while stirring vigorously. Stirring is continued for 30 minutes at room temperature. The organic phase is separated, washed twice with water, dried, filtered and evaporated. The residue is dissolved in petroleumether and the solution is decanted from some insoluble tar. The petroleumether is evaporated in vacuo. The residue is purified by column-chromatography over silica gel using trichloromethane as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from 17.5 parts of petroleumether, yielding 2.8 parts of 2,6-dichloro-α-[(2-methylphenyl)imino]benzeneacetonitrile; mp. 55° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04246429
Source datasetuspto-grants-1981_01
ORD IDord-6f0b50cbd7bd494d8dbc29f241df89df
Source noteuspto-grants-1981_01