2,2'-bis((3,5-bis(α,α'-dimethylbenzyl)-2-hydroxybenzylidene)amino)-6,6'-dimethyl-1,1'-biphenyl

Base Information

Chemical Name:2,2'-bis((3,5-bis(α,α'-dimethylbenzyl)-2-hydroxybenzylidene)amino)-6,6'-dimethyl-1,1'-biphenyl
CAS No.:1226910-12-8
Molecular Formula:C₆₄H₆₄N₂O₂
Molecular Weight:893.224
Hs Code.:

Synonyms:2,2'-bis((3,5-bis(α,α'-dimethylbenzyl)-2-hydroxybenzylidene)amino)-6,6'-dimethyl-1,1'-biphenyl

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Chemical Property of 2,2'-bis((3,5-bis(α,α'-dimethylbenzyl)-2-hydroxybenzylidene)amino)-6,6'-dimethyl-1,1'-biphenyl

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Technology Process of 2,2'-bis((3,5-bis(α,α'-dimethylbenzyl)-2-hydroxybenzylidene)amino)-6,6'-dimethyl-1,1'-biphenyl

There total 1 articles about 2,2'-bis((3,5-bis(α,α'-dimethylbenzyl)-2-hydroxybenzylidene)amino)-6,6'-dimethyl-1,1'-biphenyl which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 90.0%

: 86560-87-4,20261-65-8,3685-05-0,3685-06-1
2,2'-diamino-6,6'-dimethylbiphenyl

: 356763-82-1
2-hydroxy-3,5-dicumylbenzaldehyde

: 1226910-12-8
2,2'-bis((3,5-bis(α,α'-dimethylbenzyl)-2-hydroxybenzylidene)amino)-6,6'-dimethyl-1,1'-biphenyl

Guidance literature:: In toluene; at 110 ℃;
DOI:10.1002/ejic.200900840

Reference yield: 98.0%

: tetrakis(dimethylamido)titanium(IV)

: 75-77-4
chloro-trimethyl-silane

: 1226910-12-8
2,2'-bis((3,5-bis(α,α'-dimethylbenzyl)-2-hydroxybenzylidene)amino)-6,6'-dimethyl-1,1'-biphenyl

: cis-[TiCl2(2,2'-bis((3,5-bis(α,.alpha,'dimethylbenzyl)-2-hydroxybenzylidene)amino)-6,6-dimethyl-1,1-biphenyl(-2H))]

Guidance literature:: In toluene; Ar; ligand added to precooled toluene soln. of Ti(NMe2)4 (1:1 molar ratio), mixt. warmed to room temp., stirred overnight, concd., 10-fold excess Me3SiCl added at room temp., mixt. stirred overnight; evapd. (70°C, vac.), elem. anal.;
DOI:10.1002/ejic.200900840