N-(6-aminohexyl)-2-(4-((tert-butyldimethylsilyl)oxy)-3-methoxyphenyl)acetamide

Base Information

Chemical Name:N-(6-aminohexyl)-2-(4-((tert-butyldimethylsilyl)oxy)-3-methoxyphenyl)acetamide
CAS No.:1394822-20-8
Molecular Formula:C₂₁H₃₈N₂O₃Si
Molecular Weight:394.63
Hs Code.:

Synonyms:N-(6-aminohexyl)-2-(4-((tert-butyldimethylsilyl)oxy)-3-methoxyphenyl)acetamide

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Chemical Property of N-(6-aminohexyl)-2-(4-((tert-butyldimethylsilyl)oxy)-3-methoxyphenyl)acetamide

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Technology Process of N-(6-aminohexyl)-2-(4-((tert-butyldimethylsilyl)oxy)-3-methoxyphenyl)acetamide

There total 5 articles about N-(6-aminohexyl)-2-(4-((tert-butyldimethylsilyl)oxy)-3-methoxyphenyl)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: 100.0%

: 1394822-19-5
benzyl (6-(2-(4-((tert-butyldimethylsilyl)oxy)-3-methoxyphenyl)acetamido)hexyl)carbamate

: 1394822-20-8
N-(6-aminohexyl)-2-(4-((tert-butyldimethylsilyl)oxy)-3-methoxyphenyl)acetamide

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In methanol; at 25 ℃; for 14h;
DOI:10.1002/anie.201201451

Reference yield:

: 78324-15-9
tert-butyldimethyl 2-(4-(tert-butyldimethylsilyloxy)-3-methoxyphenyl)acetate

: 1394822-20-8
N-(6-aminohexyl)-2-(4-((tert-butyldimethylsilyl)oxy)-3-methoxyphenyl)acetamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / tetrahydrofuran / 14 h / 20 °C / Inert atmosphere

2.1: dicyclohexyl-carbodiimide / tetrahydrofuran / 14 h / 0 - 25 °C / Inert atmosphere

3.1: triethylamine / N,N-dimethyl-formamide / 0.08 h / 20 °C

3.2: 14 h / 20 °C / Inert atmosphere

4.1: palladium 10% on activated carbon; hydrogen / methanol / 14 h / 25 °C

With palladium 10% on activated carbon; hydrogen; potassium carbonate; triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1002/anie.201201451

Reference yield:

: 1344662-01-6
2-(4-((tert-butyldimethylsilyl)oxy)-3-methoxyphenyl)acetic acid

: 1394822-20-8
N-(6-aminohexyl)-2-(4-((tert-butyldimethylsilyl)oxy)-3-methoxyphenyl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: dicyclohexyl-carbodiimide / tetrahydrofuran / 14 h / 0 - 25 °C / Inert atmosphere

2.1: triethylamine / N,N-dimethyl-formamide / 0.08 h / 20 °C

2.2: 14 h / 20 °C / Inert atmosphere

3.1: palladium 10% on activated carbon; hydrogen / methanol / 14 h / 25 °C

With palladium 10% on activated carbon; hydrogen; triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1002/anie.201201451