106367-20-8

Upstream product

• 135679-54-8 2-(N-methyl)amino-4-chloro-3,3-dimethylbutanenitrile 
• 131149-78-5 2-(N-benzyl)amino-4-chloro-3,3-dimethylbutanenitrile 
• 13401-56-4 3-chloro-2,2-dimethylpropan-1-ol 
• 13401-57-5 3-chloro-2,2-dimethylpropionaldehyde 
• 100-46-9 benzylamine 

Downstream Products

• 119640-00-5 Benzyl-(3,3-dimethoxy-2,2-dimethyl-propyl)-amine 
• 119640-05-0 1-Benzyl-4-methoxy-5,5-dimethyl-tetrahydro-pyrimidine-2-thione 
• 13509-71-2 3,3-dimethyl-1-(phenylmethyl)azetidine 
• 131149-78-5 2-(N-benzyl)amino-4-chloro-3,3-dimethylbutanenitrile 
• 123445-53-4 (+/-)-2,2-dimethyl-1-aminocyclopropane-1-carboxylic acid 
• 131149-77-4 N-(benzylidene)-2,2-dimethylcyclopropanecarbonitrile 
• 131149-79-6 N-(benzylidene)-3-chloro-1-cyano-2,2-dimethylpropylamine 
• 135679-59-3 C₁₃H₁₆Cl₂N₂ 
• 109296-32-4 N-(benzylidene)-2,2-dimethylcyclopropylamine 
• 1048691-58-2 2,2-dichloro-3-(2-chloro-1,1-dimethylethyl)-1-benzylaziridine 
• 99315-29-4 1-Benzyl-3,3-dimethyl-azetidine-2-carbonitrile 
• 16047-94-2 1-Benzyl-1,3,3-trimethyl-azetidinium; iodide 

Relevant academic research and scientific papers

Synthesis of 1-amino-2,2-dialkylcyclopropanecarboxylic acids from β-chloroaldimines

A variety of hydrogen cyanide adducts of β-chloroaldimines using acetone cyanohydrin were prepared. The reactive behaviour of these α-amino-γ-chloronitriles towards bases was investigated with the aim to generate 1-aminocyclopropanecarbonitriles, which ar

SYNTHESIS OF AZETIDINES FROM β-CHLORO IMINES

The reaction of β-chloro imines 4 with potassium cyanide in methanol or with lithium aluminium hydride in dry ether gave rise to 2-cyanoazetidines 5 and azetidines 21.The reaction proceeded by nucleophilic addition of cyanide or hydride across the carbon-

Synthesis of β-Chloroimines

β-Chloroimines 6 have been prepared from β-chlorocarbonyl compounds 5 by reaction with primary amines via two major approaches.