N-(2-(4-(benzyloxy)-3-methoxyphenyl)ethyl)-2-(3,5-dimethoxyphenyl)acetamide

Base Information

Chemical Name:N-(2-(4-(benzyloxy)-3-methoxyphenyl)ethyl)-2-(3,5-dimethoxyphenyl)acetamide
CAS No.:1398120-89-2
Molecular Formula:C₂₆H₂₉NO₅
Molecular Weight:435.52
Hs Code.:

Synonyms:N-(2-(4-(benzyloxy)-3-methoxyphenyl)ethyl)-2-(3,5-dimethoxyphenyl)acetamide

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Chemical Property of N-(2-(4-(benzyloxy)-3-methoxyphenyl)ethyl)-2-(3,5-dimethoxyphenyl)acetamide

Chemical Property:

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Technology Process of N-(2-(4-(benzyloxy)-3-methoxyphenyl)ethyl)-2-(3,5-dimethoxyphenyl)acetamide

There total 5 articles about N-(2-(4-(benzyloxy)-3-methoxyphenyl)ethyl)-2-(3,5-dimethoxyphenyl)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:

: 2426-87-1
3-methoxy-4-(phenylmethoxy)benzaldehyde

: 1398120-89-2
N-(2-(4-(benzyloxy)-3-methoxyphenyl)ethyl)-2-(3,5-dimethoxyphenyl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: ammonium acetate; acetic acid / 4 h / 90 °C

2.1: lithium aluminium tetrahydride / tetrahydrofuran / 2.5 h / 0 °C / Reflux

2.2: 0 °C

3.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0.5 h / 20 °C

3.2: 8 h / 20 °C

With lithium aluminium tetrahydride; ammonium acetate; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.bmc.2012.05.057

Reference yield:

: 63909-38-6,1860-56-6
3-methoxy-4-benzyloxy-ω-nitrostyrolene

: 1398120-89-2
N-(2-(4-(benzyloxy)-3-methoxyphenyl)ethyl)-2-(3,5-dimethoxyphenyl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: lithium aluminium tetrahydride / tetrahydrofuran / 2.5 h / 0 °C / Reflux

1.2: 0 °C

2.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0.5 h / 20 °C

2.2: 8 h / 20 °C

With lithium aluminium tetrahydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.bmc.2012.05.057

Reference yield:

: 121-33-5,8014-42-4
vanillin

: 1398120-89-2
N-(2-(4-(benzyloxy)-3-methoxyphenyl)ethyl)-2-(3,5-dimethoxyphenyl)acetamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / acetone / 2 h / Reflux

2.1: ammonium acetate; acetic acid / 4 h / 90 °C

3.1: lithium aluminium tetrahydride / tetrahydrofuran / 2.5 h / 0 °C / Reflux

3.2: 0 °C

4.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0.5 h / 20 °C

4.2: 8 h / 20 °C

With lithium aluminium tetrahydride; ammonium acetate; potassium carbonate; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; dichloromethane; acetone;
DOI:10.1016/j.bmc.2012.05.057