62001-35-8

Upstream product

• 95-14-7 1,2,3-Benzotriazole 
• 50-00-0 formaldehyd 
• 95-53-4 o-toluidine 

Downstream Products

• 875-79-6 1,2-dimethylindole 
• 3558-24-5 1-methyl-2-phenyl-1H-indole 
• 51358-08-8 1-methyl-2-(4-methylphenyl)indole 
• 3558-28-9 1,3-dimethyl-2-phenyl-1H-indole 
• 1821-38-1 N-methyl-2-ethylphenylamine 
• 92645-89-1 1-phenyl-2-(2-methylaminophenyl)ethane 
• 129205-94-3 C₈H₁₀⁽²⁾HN 
• 129205-98-7 3-methyl-1-(2-methylaminophenyl)-2-butanol 
• 129205-95-4 2-n-heptyl-N-methylaniline 
• 129205-99-8 2-methylaminophenyl acetic acid t-butyl amide 
• 129206-00-4 2-methylaminophenyl acetic acid anilide 
• 129205-97-6 1-(4-methylphenyl)-2-(2-methylaminophenyl)ethanol 
• 129205-96-5 1,1-diphenyl-2-(2-methylaminophenyl)ethanol 
• 611-21-2 N,2-dimethylaniline 

Relevant academic research and scientific papers

Substituent effects in the bis(benzotriazolylmethylation) of aromatic amines

1-(Hydroxymethyl)benzotriazole and aromatic amines react to give an equilibrium mixture of N-mono- and N,N-bis(benzotriazolylmethyl)arylamines.Electron-releasing substituents on the arylamine ring shift the equilibrium towards the N,N-bis(benzotriazolylme

CARBON DIOXIDE: A REAGENT FOR THE SIMULTANEOUS PROTECTION OF NUCLEOPHILIC CENTERS AND THE ACTIVATION OF ALTERNATIVE LOCATIONS TO ELECTROPHILIC ATTACK. 16. A NOVEL SYNTHETIC METHOD FOR THE SIDE-CHAIN FUNCTIONALIZATION OF N-METHYL-o-TOLUIDINE AND FOR THE PREPARATION OF 2-SUBSTITUTED...

N-Methyl-o-toluidine is readily converted into a range of side-chain functionalized derivatives in a one-pot sequence, using carbon dioxide for N-protection.The intermediate lithium carbamate is further lithiated by butyllithium at the side-chain methyl group, and then reacted with an electrophile; the product undergoes acid-catalyzed decarboxylation during work-up. 2-Substituted N-methylindoles are produced when carboxylate esters are used as electrophiles.The yields are good, and no ring-substituted products are detected.