40171-95-7

Usage

InChI:InChI=1/C11H17NO2/c1-4-12-8-9-5-6-10(13-2)11(7-9)14-3/h5-7,12H,4,8H2,1-3H3

Upstream product

• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 75-04-7 ethylamine 
• 65609-25-8 N-acetyl-3,4-dimethoxybenzylamine 
• 5763-61-1 3,4-dimethoxybenzylamine 

Downstream Products

• 101438-80-6 5-(ethyl-veratryl-amino)-valeronitrile 
• 103044-23-1 N-ethyl-N'-(3,4-dimethoxy-phenethyl)-N-veratryl-pentanediyldiamine 
• 102179-78-2 N-ethyl-N'-isopropyl-N-veratryl-pentanediyldiamine 
• 101725-29-5 N-ethyl-N-veratryl-pentanediyldiamine 
• 112690-29-6 N-ethyl-N'-tetrahydrofurfuryl-N-veratryl-pentanediyldiamine 

Relevant academic research and scientific papers

Application of the ortho-Lithiation-Cyclization Strategy to N-Benzyl- and N-Phenethylamine Derivatives

The ortho-lithiation-cyclization of iodinated N,N-diacylphenethylamines provides a convenient method for the preparation of 2-(2-acetoamidoethyl)acetophenones and 2-(2-benzamidoethyl)benzophenones, which could be easily transformed into dihydroisoquinolines.By contrast, the N-ethylamino, N-acetylamino, and N-trimethylsilylamino moieties studied as ortho-directing groups provide poor assistance to the metalation of N-benzyl- and N-phenyethylamines and the corresponding isoindolone or isoquinolone derivatives are obtained in low yields.