tert-butyl 2-{[(R)-2-(tert-butyldiphenylsilyloxy)-1-phenylethylamino]methyl}phenylcarbamate

Base Information

Chemical Name:tert-butyl 2-{[(R)-2-(tert-butyldiphenylsilyloxy)-1-phenylethylamino]methyl}phenylcarbamate
CAS No.:855307-25-4
Molecular Formula:C₃₆H₄₄N₂O₃Si
Molecular Weight:580.842
Hs Code.:

Synonyms:tert-butyl 2-{[(R)-2-(tert-butyldiphenylsilyloxy)-1-phenylethylamino]methyl}phenylcarbamate

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Chemical Property of tert-butyl 2-{[(R)-2-(tert-butyldiphenylsilyloxy)-1-phenylethylamino]methyl}phenylcarbamate

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Technology Process of tert-butyl 2-{[(R)-2-(tert-butyldiphenylsilyloxy)-1-phenylethylamino]methyl}phenylcarbamate

There total 6 articles about tert-butyl 2-{[(R)-2-(tert-butyldiphenylsilyloxy)-1-phenylethylamino]methyl}phenylcarbamate 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: 66.0%

: 855307-24-3
2-{[(R)-2-(2-tert-butyldiphenylsilyloxy)-1-phenylethylamino]methyl}phenylamine

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

: 855307-25-4
tert-butyl 2-{[(R)-2-(tert-butyldiphenylsilyloxy)-1-phenylethylamino]methyl}phenylcarbamate

Guidance literature:: 2-{[(R)-2-(2-tert-butyldiphenylsilyloxy)-1-phenylethylamino]methyl}phenylamine; With sodium hydride; In tetrahydrofuran; at 0 ℃; for 0.25h;

di-tert-butyl dicarbonate; In tetrahydrofuran; at 20 ℃; for 18h;
DOI:10.1002/ejoc.200400682

Reference yield:

: (R)-2-{[1-(2-Nitro-phenyl)-meth-(E)-ylidene]-amino}-2-phenyl-ethanol

: 855307-25-4
tert-butyl 2-{[(R)-2-(tert-butyldiphenylsilyloxy)-1-phenylethylamino]methyl}phenylcarbamate

Guidance literature:: Multi-step reaction with 4 steps

1.1: 8.2 g / NaBH₄ / methanol / 20 °C

2.1: 83 percent / hydrogen / Pd/C / ethanol / 18 h / 20 °C / 760 Torr

3.1: 72 percent / imidazole / dimethylformamide / 18 h / 20 °C

4.1: NaH / tetrahydrofuran / 0.25 h / 0 °C

4.2: 66 percent / tetrahydrofuran / 18 h / 20 °C

With 1H-imidazole; sodium tetrahydroborate; hydrogen; sodium hydride; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide;
DOI:10.1002/ejoc.200400682

Reference yield:

: 855307-22-1
(R)-2-(2-nitrobenzylamino)-2-phenylethanol

: 855307-25-4
tert-butyl 2-{[(R)-2-(tert-butyldiphenylsilyloxy)-1-phenylethylamino]methyl}phenylcarbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: 83 percent / hydrogen / Pd/C / ethanol / 18 h / 20 °C / 760 Torr

2.1: 72 percent / imidazole / dimethylformamide / 18 h / 20 °C

3.1: NaH / tetrahydrofuran / 0.25 h / 0 °C

3.2: 66 percent / tetrahydrofuran / 18 h / 20 °C

With 1H-imidazole; hydrogen; sodium hydride; palladium on activated charcoal; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide;
DOI:10.1002/ejoc.200400682