N-(5-benzyloxy-2-bromo-4-methoxybenzyl)-N-methyl-(4-benzyloxyphenyl)acetamide

Base Information

Chemical Name:N-(5-benzyloxy-2-bromo-4-methoxybenzyl)-N-methyl-(4-benzyloxyphenyl)acetamide
CAS No.:32293-48-4
Molecular Formula:C₃₁H₃₀BrNO₄
Molecular Weight:560.487
Hs Code.:

Synonyms:N-(5-benzyloxy-2-bromo-4-methoxybenzyl)-N-methyl-(4-benzyloxyphenyl)acetamide

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Chemical Property of N-(5-benzyloxy-2-bromo-4-methoxybenzyl)-N-methyl-(4-benzyloxyphenyl)acetamide

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Technology Process of N-(5-benzyloxy-2-bromo-4-methoxybenzyl)-N-methyl-(4-benzyloxyphenyl)acetamide

There total 7 articles about N-(5-benzyloxy-2-bromo-4-methoxybenzyl)-N-methyl-(4-benzyloxyphenyl)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: 93.0%

: 330800-27-6
N-(5-benzyloxy-2-bromo-4-methoxybenzyl)-(4-benzyloxyphenyl)acetamide

: 74-88-4
methyl iodide

: 32293-48-4
N-(5-benzyloxy-2-bromo-4-methoxybenzyl)-N-methyl-(4-benzyloxyphenyl)acetamide

Guidance literature:: With sodium hydrate; In N,N-dimethyl-formamide; at 20 ℃; for 2h;
DOI:10.1021/ol0155337

Reference yield:

: 13255-21-5
1-(benzyloxy)-4-bromo-5-(chloromethyl)-2-methoxybenzene

: 32293-48-4
N-(5-benzyloxy-2-bromo-4-methoxybenzyl)-N-methyl-(4-benzyloxyphenyl)acetamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: NaN₃ / dimethylformamide / 1 h / 20 °C

2.1: Ph₃P / tetrahydrofuran / 3 h / 20 °C

2.2: 89 percent / H₂O / tetrahydrofuran / 5 h / 70 °C

3.1: 87 percent / sodium hydrogen carbonate / diethyl ether / 2 h

4.1: 93 percent / sodium hydrate / dimethylformamide / 2 h / 20 °C

With sodium azide; sodium hydrate; sodium hydrogencarbonate; triphenylphosphine; In tetrahydrofuran; diethyl ether; N,N-dimethyl-formamide;
DOI:10.1021/ol0155337

Reference yield:

: 13397-01-8
[5-(benzyloxy)-2-bromo-4-methoxyphenyl]methanol

: 32293-48-4
N-(5-benzyloxy-2-bromo-4-methoxybenzyl)-N-methyl-(4-benzyloxyphenyl)acetamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: 100 percent / thionyl chloride / benzene / 1 h / Heating

2.1: NaN₃ / dimethylformamide / 1 h / 20 °C

3.1: Ph₃P / tetrahydrofuran / 3 h / 20 °C

3.2: 89 percent / H₂O / tetrahydrofuran / 5 h / 70 °C

4.1: 87 percent / sodium hydrogen carbonate / diethyl ether / 2 h

5.1: 93 percent / sodium hydrate / dimethylformamide / 2 h / 20 °C

With thionyl chloride; sodium azide; sodium hydrate; sodium hydrogencarbonate; triphenylphosphine; In tetrahydrofuran; diethyl ether; N,N-dimethyl-formamide; benzene;
DOI:10.1021/ol0155337