Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350912Generated: October 25, 2026

2,6-Dichlorobenzaldehyde → (3-Chloro-1,1-dimethylpropyl)-(2,6-dichlorobenzylidene)-amine

https://huagongshe.com/reaction/1350912

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DichlorobenzaldehydeHCID 6737—
ReactantSodium HydroxideHCID 14798—
Reactant4-Chloro-2-methylbutan-2-amine hydrochlorideHCID 21094547—
SolventDichloromethaneHCID 6344—
Product(3-Chloro-1,1-dimethylpropyl)-(2,6-dichlorobenzylidene)-amineHCID 2109454699%

Reaction Conditions

Temperature0 °C

Reaction Steps

13.3 g (84.0 mmol) of 3-chloro-1,1-dimethyl propylamine-hydrochloride were added to 84.0 mL sodium hydroxide solution (1 M) at 0° C. with vigorous stirring. The reaction mixture was stirred for 30 min at 0° C. and then combined with 50 mL methylene chloride. The phases were separated and the aqueous phase was twice extracted with 35 mL methylene chloride. The combined organic phases were dried over magnesium sulphate and at ambient temperature combined with 14.2 g (81.0 mmol) of 2,6-dichlorobenzaldehyde with stirring. The reaction mixture was stirred for 18 h at ambient temperature, dried again with magnesium sulphate and the solvent was removed. 22.3 g (80.0 mmol, 99%) (3-chloro-1,1-dimethylpropyl)-(2,6-dichlorobenzylidene)-amine were obtained as a yellowish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214698B2
Source datasetuspto-grants-2007_05
ORD IDord-97b6c5badb5e4b48ab2cce294e41862e
Source noteuspto-grants-2007_05