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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262195Generated: October 30, 2026

3,4-Dichlorobenzyl chloride → HCID 21320353, compound

https://huagongshe.com/reaction/262195

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dichlorobenzyl chlorideHCID 7609—
ReactantPropanedinitrile, [[[3,5-bis(trifluoromethyl)phenyl]amino]methylene]-HCID 2797077—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 21320353HCID 21320353—

Reaction Steps

With stirring, 16.8 g of potassium tert-butylate are added by small amounts to a solution of 45.7 g of 3,5-bis-trifluoromethyl-N-(2,2-dicyanovinyl)-aniline in 200 ml of dimethyl sulphoxide. The solution is kept for 4 hours at 40° C. With further stirring, 20.8 ml of 3,4-dichlorobenzyl chloride in 20 ml of dimethyl sulphoxide are added dropwise and the reaction mixture is then stirred for 12 hours at 40° C. The mixture is then poured onto 2 liters of ice and the precipitated product is extracted with chloroform. The chloroform solution is washed with water, dried over sodium sulphate and the chloroform is distilled off. The crude product is chromatographed over a silica gel column with methyl acetate/hexane (1:3 v/v) as eluant, yielding 15 g of the desired product in the form of yellow crystals with a melting point of 102°-103° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04153723
Source datasetuspto-grants-1979_05
ORD IDord-225acab61f51469e8127b050b0112051
Source noteuspto-grants-1979_05