121059-40-3

Upstream product

• 52387-40-3 5-chloro-2,2-dimethylpentanal 
• 100-46-9 benzylamine 
• 121059-33-4 tert-Butyl-[6-chloro-2,2-dimethyl-hex-(E)-ylidene]-amine 
• 121059-31-2 N-tert-Butyl-5-chloro-2,2-dimethylpentanimine 
• 121059-32-3 [5-Chloro-2,2-dimethyl-pent-(E)-ylidene]-isopropyl-amine 

Downstream Products

• 125943-32-0 1-Benzyl-3,3-dimethyl-piperidine-2-carbonitrile 
• 125943-36-4 3,3-dimethyl-1-(phenylmethyl)piperidine 
• 125966-59-8 (5-Chloro-2,2-dimethyl-pentyl)-[1-phenyl-meth-(Z)-ylidene]-amine 
• 125966-58-7 (3,3-Dimethyl-piperidin-1-yl)-phenyl-acetonitrile 

Relevant academic research and scientific papers

Preparation of ω-Chloroimines

Alkylation of 1-azaallylic anions (generated by deprotonation of alkanimines) with 1,ω-dihaloalkanes provides a useful procedure for the synthesis of δ-chloro- and ε-chloroalkanimines.These ω-haloalkanimines have not been isolated and characterized before, although some representatives were already used as intermediates in some transformations.