N-(5-benzyloxy-2-bromo-4-methoxy-phenyl)-3-(4-benzyloxy-phenyl)-N-methyl-propionamide

Base Information

Chemical Name:N-(5-benzyloxy-2-bromo-4-methoxy-phenyl)-3-(4-benzyloxy-phenyl)-N-methyl-propionamide
CAS No.:862794-40-9
Molecular Formula:C₃₁H₃₀BrNO₄
Molecular Weight:560.487
Hs Code.:

<i>N</i>-(5-benzyloxy-2-bromo-4-methoxy-phenyl)-3-(4-benzyloxy-phenyl)-<i>N</i>-methyl-propionamide

Synonyms:N-(5-benzyloxy-2-bromo-4-methoxy-phenyl)-3-(4-benzyloxy-phenyl)-N-methyl-propionamide

Suppliers and Price of N-(5-benzyloxy-2-bromo-4-methoxy-phenyl)-3-(4-benzyloxy-phenyl)-N-methyl-propionamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-(5-benzyloxy-2-bromo-4-methoxy-phenyl)-3-(4-benzyloxy-phenyl)-N-methyl-propionamide

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Technology Process of N-(5-benzyloxy-2-bromo-4-methoxy-phenyl)-3-(4-benzyloxy-phenyl)-N-methyl-propionamide

There total 10 articles about N-(5-benzyloxy-2-bromo-4-methoxy-phenyl)-3-(4-benzyloxy-phenyl)-N-methyl-propionamide 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:

: 5597-50-2
3-(4-hydroxyphenyl)propionic acid methyl ester

: 862794-40-9
N-(5-benzyloxy-2-bromo-4-methoxy-phenyl)-3-(4-benzyloxy-phenyl)-N-methyl-propionamide

Guidance literature:: Multi-step reaction with 4 steps

1: 92 percent / K₂CO₃ / dimethylformamide / 18 h / 120 °C

2: 90 percent / aq. KOH / methanol / 60 °C

3: 100 percent / thionyl chloride / 2 h / Heating

4: 23.8 g / Et₃N / CHCl₃ / 1 h

With potassium hydroxide; thionyl chloride; potassium carbonate; triethylamine; In methanol; chloroform; N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2005.05.055

Reference yield:

: 862794-16-9
3-hydroxy-4-methoxyformanilide

: 862794-40-9
N-(5-benzyloxy-2-bromo-4-methoxy-phenyl)-3-(4-benzyloxy-phenyl)-N-methyl-propionamide

Guidance literature:: Multi-step reaction with 4 steps

1: 82 percent / K₂CO₃ / dimethylformamide / 8 h / 120 °C

2: 86 percent / N-bromoacetamide / tetrahydrofuran / 0 °C

3: 91 percent / BH₃*THF / tetrahydrofuran / 0.5 h / Heating

4: 23.8 g / Et₃N / CHCl₃ / 1 h

With borane-THF; potassium carbonate; triethylamine; N-bromoacetamide; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2005.05.055

Reference yield:

: 862794-18-1
3-benzyloxy-4-methoxyformanilide

: 862794-40-9
N-(5-benzyloxy-2-bromo-4-methoxy-phenyl)-3-(4-benzyloxy-phenyl)-N-methyl-propionamide

Guidance literature:: Multi-step reaction with 3 steps

1: 86 percent / N-bromoacetamide / tetrahydrofuran / 0 °C

2: 91 percent / BH₃*THF / tetrahydrofuran / 0.5 h / Heating

3: 23.8 g / Et₃N / CHCl₃ / 1 h

With borane-THF; triethylamine; N-bromoacetamide; In tetrahydrofuran; chloroform;
DOI:10.1016/j.tet.2005.05.055