57675-92-0

Upstream product

• 136918-14-4 phthalimide 
• 50-00-0 formaldehyd 
• 103-67-3 benzyl-methyl-amine 
• 103-83-3 N,N'-dimethylbenzylamine 

Downstream Products

• 23873-65-6 3-(N-benzyl-N-methylamino)propionitrile 
• 57675-84-0 3-(Benzyl-methyl-amino)-2-[(benzyl-methyl-amino)-methyl]-propionitrile 
• 57675-91-9 N-Methyl-N-(2,2,2-trichlorethyl)benzylamin 
• 74873-99-7 N-(N'-Benzyl-N'-methylaminomethyl)-3-hydroxyisoindolin-1-one 
• 74066-71-0 1,2,3,9b-tetrahydro-9b-hydroxy-2-methyl-1-phenylimidazo<4,3-a>isoindol-5-one 

Relevant academic research and scientific papers

Electrochemical Dehydrogenative Imidation of N-Methyl-Substituted Benzylamines with Phthalimides for the Direct Synthesis of Phthalimide-Protected gem-Diamines

A general and green electrochemical dehydrogenative method for the imidation of N-methyl benzylamines with phthalimides with excellent regioselectivities is reported for the first time. This operationally simple method offers a valuable tool to obtain str

Photochemical Cyclisation of Phthalimide Mannich Bases

Ultraviolet irradiation of Mannich bases derived from phthalimide, formaldehyde, and a secondary amine leads to cyclised products containing a new imidazolidine ring.The reaction is much less efficient when the secondary amine has an aromatic group adjacent to the nitrogen atom.Exceptionally, the Mannich base derived from 3-pyrroline does not cyclise but undergoes an internal oxidation-reduction reaction to give a substituted pyrrole.