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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350911Generated: October 26, 2026

Dimethylformamide → Dichlorobenzylidenamine

https://huagongshe.com/reaction/1350911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2,6-DichlorobenzaldehydeHCID 6737—
Reactant4-Chloro-2-methylbutan-2-amine hydrochlorideHCID 21094547—
SolventDimethyl SulfoxideHCID 679—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventDiethylethyletherHCID 12430074—
ProductDichlorobenzylidenamineHCID 131726441—

Reaction Steps

The base is liberated from about 80–90, preferably 84.0 mmol of 3-chloro-1,1-dimethylpropylamine-hydrochloride by known methods. The free base is dissolved in about 50 mL of a solvent, preferably toluene, diethylethylether, tetrahydrofuran, dimethylsulphoxide, dimethylformamide or methylene chloride and about 60 to 100 mmol, preferably 80.0 mmol of 2,6-dichlorobenzaldehyde are added at ambient temperature, with stirring. The reaction mixture is stirred for 5 to 20 h, preferably for 15 h at ambient temperature, dried again and the solvent is removed. The corresponding dichlorobenzylidenamine of compound (III) is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214698B2
Source datasetuspto-grants-2007_05
ORD IDord-6af98bf814c24801a9689cef8d7e3e26
Source noteuspto-grants-2007_05