2-bromo-N-[2-(tert-butyl-dimethyl-silanyloxy)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(4-nitro-phenyl)-ethyl]-acetamide

Base Information

Chemical Name:2-bromo-N-[2-(tert-butyl-dimethyl-silanyloxy)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(4-nitro-phenyl)-ethyl]-acetamide
CAS No.:519182-59-3
Molecular Formula:C₂₃H₄₁BrN₂O₅Si₂
Molecular Weight:561.664
Hs Code.:

2-bromo-<i>N</i>-[2-(<i>tert</i>-butyl-dimethyl-silanyloxy)-1-(<i>tert</i>-butyl-dimethyl-silanyloxymethyl)-2-(4-nitro-phenyl)-ethyl]-acetamide

Synonyms:2-bromo-N-[2-(tert-butyl-dimethyl-silanyloxy)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(4-nitro-phenyl)-ethyl]-acetamide

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Chemical Property of 2-bromo-N-[2-(tert-butyl-dimethyl-silanyloxy)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(4-nitro-phenyl)-ethyl]-acetamide

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Technology Process of 2-bromo-N-[2-(tert-butyl-dimethyl-silanyloxy)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(4-nitro-phenyl)-ethyl]-acetamide

There total 4 articles about 2-bromo-N-[2-(tert-butyl-dimethyl-silanyloxy)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(4-nitro-phenyl)-ethyl]-acetamide 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:

: 69739-34-0
t-butyldimethylsiyl triflate

: 519182-59-3
2-bromo-N-[2-(tert-butyl-dimethyl-silanyloxy)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(4-nitro-phenyl)-ethyl]-acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: 97 percent / 2,6-lutidine / CH₂Cl₂ / 4 h / 0 °C

2: 98 percent / piperidine / dimethylformamide / 1 h / 20 °C

3: 95 percent / pyridine / CH₂Cl₂ / 1 h / 0 °C

With piperidine; pyridine; 2,6-dimethylpyridine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ja038937y

Reference yield:

: 119-62-0,716-61-0,2792-51-0,2792-52-1,2964-48-9,3689-55-2,63526-31-8,71115-69-0,140694-64-0
(1R,2R)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol

: 519182-59-3
2-bromo-N-[2-(tert-butyl-dimethyl-silanyloxy)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(4-nitro-phenyl)-ethyl]-acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / aq. NaHCO₃ / diethyl ether / 24 h / 20 °C

2: 97 percent / 2,6-lutidine / CH₂Cl₂ / 4 h / 0 °C

3: 98 percent / piperidine / dimethylformamide / 1 h / 20 °C

4: 95 percent / pyridine / CH₂Cl₂ / 1 h / 0 °C

With piperidine; pyridine; 2,6-dimethylpyridine; sodium hydrogencarbonate; In diethyl ether; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ja038937y

Reference yield:

: 533914-87-3
[(1R,2R)-2-Hydroxy-1-hydroxymethyl-2-(4-nitro-phenyl)-ethyl]-carbamic acid 9H-fluoren-9-ylmethyl ester

: 519182-59-3
2-bromo-N-[2-(tert-butyl-dimethyl-silanyloxy)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(4-nitro-phenyl)-ethyl]-acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: 97 percent / 2,6-lutidine / CH₂Cl₂ / 4 h / 0 °C

2: 98 percent / piperidine / dimethylformamide / 1 h / 20 °C

3: 95 percent / pyridine / CH₂Cl₂ / 1 h / 0 °C

With piperidine; pyridine; 2,6-dimethylpyridine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ja038937y