117568-53-3

Upstream product

• 50-00-0 formaldehyd 
• 64-04-0 phenethylamine 
• 171920-10-8 N,N-bis(ethoxymethyl)-β-phenylethylamine 
• 156-28-5 2-phenylethylamine hydrochloride 

Downstream Products

• 873303-61-8 [(1,3,5-triphenylethyl-1,3,5-triazacyclohexane)trichlorotitanium(IV)] tetrakis(pentafluoro)borate 
• 635685-08-4 [((CH₂N(C₂H₄C₆H₅))3)CrCl₃]*[C₆H₅N(CH₃)2H]⁽¹⁺⁾*[B(C₆F₅)4]^(1-)=[((CH₂N(C₂H₄C₆H₅))3)CrCl₃][C₆H₅N(CH₃)2H][B(C₆F₅)4] 
• 873303-49-2 [(1,3,5-triphenylethyl-1,3,5-triazacyclohexane)trichlorotitanium(IV)] nonachlorodititanate(IV) 
• 371238-49-2 [((CH₂N(C₂H₄C₆H₅))3)CrCl₃] 
• 63235-61-0 4,5-diphenyl-1-(2-phenylethyl)imidazole 3-oxide 

Relevant academic research and scientific papers

Role of hydroxyl groups on the aromatic ring in the reactivity and selectivity of the reaction of β -phenylethylamines with non-enolizable aldehydes

The influence of hydroxyl groups on the β-phenylethylamine aromatic ring was studied during its reaction with non-enolizable aldehydes. Computational calculations established that the degree of hydroxylation generates differences in the activation pattern

The Synthesis of 2-Arylmethyltetrahydroisoquinolines from Bis(Aminol) Ethers Involving Two Iminium Salt Intermediates

The bis(aminol) ether derived from 3,4-dimethoxy-β-phenylethylamine, methanol, and formaldehyde reacts with trichloromethylsilane to afford an equilibrium mixture of N-chloromethyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline and its related iminium chloride.Interaction with electron rich aromatic compounds afford good yields of N-arylmethyl derivatives, including sendaverine methyl ether.Reactions of the bis(amino) ether in the presence of the aromatic substrate allows the formation of the N-arylmethyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline derivatives in a one pot reaction.