tert-butyl (R)-(2-(3-aminophenyl)-2-((triethylsilyl)oxy)ethyl)(2-hydroxyethyl)carbamate

Base Information

Chemical Name:tert-butyl (R)-(2-(3-aminophenyl)-2-((triethylsilyl)oxy)ethyl)(2-hydroxyethyl)carbamate
CAS No.:1221179-27-6
Molecular Formula:C₂₁H₃₈N₂O₄Si
Molecular Weight:410.629
Hs Code.:

Synonyms:tert-butyl (R)-(2-(3-aminophenyl)-2-((triethylsilyl)oxy)ethyl)(2-hydroxyethyl)carbamate

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Chemical Property of tert-butyl (R)-(2-(3-aminophenyl)-2-((triethylsilyl)oxy)ethyl)(2-hydroxyethyl)carbamate

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Technology Process of tert-butyl (R)-(2-(3-aminophenyl)-2-((triethylsilyl)oxy)ethyl)(2-hydroxyethyl)carbamate

There total 6 articles about tert-butyl (R)-(2-(3-aminophenyl)-2-((triethylsilyl)oxy)ethyl)(2-hydroxyethyl)carbamate 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:

: 24424-99-5
di-tert-butyl dicarbonate

: 1221179-26-5
(R)-N-benzyl-N-(2-(benzyloxy)ethyl)-2-(3-nitrophenyl)-2-((triethylsilyl)oxy)ethan-1-amine

: 1221179-27-6
tert-butyl (R)-(2-(3-aminophenyl)-2-((triethylsilyl)oxy)ethyl)(2-hydroxyethyl)carbamate

Guidance literature:: (R)-N-benzyl-N-(2-(benzyloxy)ethyl)-2-(3-nitrophenyl)-2-((triethylsilyl)oxy)ethan-1-amine; With hydrogen; palladium 10% on activated carbon; In ethanol; water; at 50 ℃; for 13h;

di-tert-butyl dicarbonate; In tetrahydrofuran; at 20 ℃; for 1.5h;

With hydrogen; 20 % Pd(OH)2/C; In tetrahydrofuran; methanol; water; at 50 ℃; for 8h;

Reference yield:

: 1221179-25-4
(R)-2-(N-benzyl-N-(2-(benzyloxy)ethyl)amino)-1-(3-nitrophenyl)ethan-1-ol

: 1221179-27-6
tert-butyl (R)-(2-(3-aminophenyl)-2-((triethylsilyl)oxy)ethyl)(2-hydroxyethyl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1.1: 1H-imidazole / N,N-dimethyl-formamide / 20 °C

2.1: hydrogen / palladium 10% on activated carbon / ethanol; water / 13 h / 50 °C

2.2: 1.5 h / 20 °C

2.3: 8 h / 50 °C

With 1H-imidazole; hydrogen; palladium 10% on activated carbon; In ethanol; water; N,N-dimethyl-formamide;