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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838664Generated: November 2, 2026

3-(2,6-Dichloro-4-trifluoromethylphenylhydrazino)propionitrile → HCID 21982150, compound

https://huagongshe.com/reaction/1838664

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(2,6-Dichloro-4-trifluoromethylphenylhydrazino)propionitrileHCID 11087805—
Reactant3-{2-[2,6-Dichloro-4-(trifluoromethyl)phenyl]hydrazinylidene}propanenitrileHCID 69551700—
SolventChlorobenzeneHCID 7964—
ProductHCID 21982150HCID 21982150—
Product3-{2-[2,6-Dichloro-4-(trifluoromethyl)phenyl]hydrazinylidene}propanenitrileHCID 69551700—

Reaction Conditions

Temperature65 °C

Reaction Steps

Preparation of 3-(2,6-dichloro-4-trifluoromethylphenylhydrazono)propionitrile from 3-(2,6-dichloro-4-trifluoromethylphenylhydrazino)propionitrile Cupric chloride (0.673 g, 2.5 equivalents) was added in one portion to a solution of 3-(2,6-dichloro-4-trifluoromethylphenylhydrazino)propionitrile (0.591 g, 2 mmol) in chlorobenzene, and the mixture heated at 65° C. for 50 minutes. The reaction was judged to be complete and was cooled, washed (water), dried (magnesium sulfate), evaporated and separated by chromatography on silica gel to give 3-(2,6-dichloro-4-trifluoromethylphenylhydrazono)propionitrile, NMR 3.37 (d, 2H), 7.03 (t, 1H), 7.5 (s, 2H), 7.75 (s, 1H) (35% yield), and 3-(2,6-dichloro-4-trifluoromethylphenylazo)propionitrile, NMR 3.0 (t, 2H), 4.6 (t, 2H), 7.6 (s, 2H) (60% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06673956B2
Source datasetuspto-grants-2004_01
ORD IDord-4a8704bec97b4d14b50be84525106a87
Source noteuspto-grants-2004_01