N-(2-(benzyloxy)-5-methoxybenzyl)-2-bromo-N-(2-phenoxyphenyl)acetamide

Base Information

• Chemical Name: N-(2-(benzyloxy)-5-methoxybenzyl)-2-bromo-N-(2-phenoxyphenyl)acetamide
• CAS No.: 1334484-11-5
• Molecular Formula: C₂₉H₂₆BrNO₄
• Molecular Weight: 532.434
• Mol file: 1334484-11-5.mol

Synonyms:N-(2-(benzyloxy)-5-methoxybenzyl)-2-bromo-N-(2-phenoxyphenyl)acetamide

Chemical Property of N-(2-(benzyloxy)-5-methoxybenzyl)-2-bromo-N-(2-phenoxyphenyl)acetamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-(2-(benzyloxy)-5-methoxybenzyl)-2-bromo-N-(2-phenoxyphenyl)acetamide

There total 5 articles about N-(2-(benzyloxy)-5-methoxybenzyl)-2-bromo-N-(2-phenoxyphenyl)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: 86.0%

N-(2-(benzyloxy)-5-methoxybenzyl)-2-phenoxyaniline (1334484-10-4) + 2-Bromoacetyl bromide (598-21-0) → N-(2-(benzyloxy)-5-methoxybenzyl)-2-bromo-N-(2-phenoxyphenyl)acetamide (1334484-11-5)

Guidance literature:

With triethylamine; In dichloromethane; at 0 - 20 ℃;

DOI:10.1016/j.steroids.2011.06.012

Reference yield:

C27H23NO3 → N-(2-(benzyloxy)-5-methoxybenzyl)-2-bromo-N-(2-phenoxyphenyl)acetamide (1334484-11-5)

Guidance literature:

Multi-step reaction with 2 steps

1: sodium tetrahydroborate / methanol / 0 - 20 °C / Inert atmosphere

2: triethylamine / dichloromethane / 0 - 20 °C

With sodium tetrahydroborate; triethylamine; In methanol; dichloromethane;

DOI:10.1016/j.steroids.2011.06.012

Reference yield:

2-hydroxy-5-methoxybenzaldehyde (672-13-9) → N-(2-(benzyloxy)-5-methoxybenzyl)-2-bromo-N-(2-phenoxyphenyl)acetamide (1334484-11-5)

Guidance literature:

Multi-step reaction with 4 steps

1: potassium carbonate / N,N-dimethyl-formamide / 5 h / 45 °C

2: 4 h / 20 - 95 °C / Inert atmosphere

3: sodium tetrahydroborate / methanol / 0 - 20 °C / Inert atmosphere

4: triethylamine / dichloromethane / 0 - 20 °C

With sodium tetrahydroborate; potassium carbonate; triethylamine; In methanol; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1016/j.steroids.2011.06.012

upstream raw materials:

2-hydroxy-5-methoxybenzaldehyde

N-(2-(benzyloxy)-5-methoxybenzyl)-2-phenoxyaniline

2-Bromoacetyl bromide

2-benzyloxy-5-methoxybenzaldehyde

Downstream raw materials:

N-(2-(benzyloxy)-5-methoxybenzyl)-2-fluoro-N-(2-phenoxyphenyl)acetamide

2-fluoro-N-(2-hydroxy-5-methoxybenzyl)-N-(2-phenoxyphenyl)-acetamide