[2-(tert-butyldimethylsilanyloxy)ethyl]-[4-(1H-indol-2-yl)phenyl](methyl)amine

Base Information

Chemical Name:[2-(tert-butyldimethylsilanyloxy)ethyl]-[4-(1H-indol-2-yl)phenyl](methyl)amine
CAS No.:1442656-88-3
Molecular Formula:C₂₃H₃₂N₂OSi
Molecular Weight:380.605
Hs Code.:

Synonyms:[2-(tert-butyldimethylsilanyloxy)ethyl]-[4-(1H-indol-2-yl)phenyl](methyl)amine

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Chemical Property of [2-(tert-butyldimethylsilanyloxy)ethyl]-[4-(1H-indol-2-yl)phenyl](methyl)amine

Chemical Property:

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Technology Process of [2-(tert-butyldimethylsilanyloxy)ethyl]-[4-(1H-indol-2-yl)phenyl](methyl)amine

There total 6 articles about [2-(tert-butyldimethylsilanyloxy)ethyl]-[4-(1H-indol-2-yl)phenyl](methyl)amine 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: 60.0%

: 1442656-87-2
2-[4-(1H-indol-2-yl)-phenyl](methyl)aminoethanol

: 18162-48-6
tert-butyldimethylsilyl chloride

: 1442656-88-3
[2-(tert-butyldimethylsilanyloxy)ethyl]-[4-(1H-indol-2-yl)phenyl](methyl)amine

Guidance literature:: With 1H-imidazole; In dichloromethane; at 40 ℃; for 0.166667h;
DOI:10.1016/j.bmc.2013.04.028

Reference yield:

: 17687-47-7
mono-N-methylaminoacetophenone

: 1442656-88-3
[2-(tert-butyldimethylsilanyloxy)ethyl]-[4-(1H-indol-2-yl)phenyl](methyl)amine

Guidance literature:: Multi-step reaction with 3 steps

1: polyphosphoric acid / 0.17 h / 130 °C

2: potassium n-butoxide; potassium iodide / acetonitrile / 72 h / 80 °C

3: 1H-imidazole / dichloromethane / 0.17 h / 40 °C

With 1H-imidazole; potassium n-butoxide; potassium iodide; In dichloromethane; acetonitrile;
DOI:10.1016/j.bmc.2013.04.028

Reference yield:

: 1252037-82-3
4-(1H-indol-2-yl)-N-methylbenzenenamine

: 1442656-88-3
[2-(tert-butyldimethylsilanyloxy)ethyl]-[4-(1H-indol-2-yl)phenyl](methyl)amine

Guidance literature:: Multi-step reaction with 2 steps

1: potassium n-butoxide; potassium iodide / acetonitrile / 72 h / 80 °C

2: 1H-imidazole / dichloromethane / 0.17 h / 40 °C

With 1H-imidazole; potassium n-butoxide; potassium iodide; In dichloromethane; acetonitrile;
DOI:10.1016/j.bmc.2013.04.028