2-(3,4,5-trimethoxyphenyl)-2-acetoxy-N-methyl-N-(1-(3-methoxyphenyl)ethyl)-acetamide

Base Information

Chemical Name:2-(3,4,5-trimethoxyphenyl)-2-acetoxy-N-methyl-N-(1-(3-methoxyphenyl)ethyl)-acetamide
CAS No.:929048-90-8
Molecular Formula:C₂₃H₂₉NO₇
Molecular Weight:431.486
Hs Code.:

Synonyms:2-(3,4,5-trimethoxyphenyl)-2-acetoxy-N-methyl-N-(1-(3-methoxyphenyl)ethyl)-acetamide

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Chemical Property of 2-(3,4,5-trimethoxyphenyl)-2-acetoxy-N-methyl-N-(1-(3-methoxyphenyl)ethyl)-acetamide

Chemical Property:

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Technology Process of 2-(3,4,5-trimethoxyphenyl)-2-acetoxy-N-methyl-N-(1-(3-methoxyphenyl)ethyl)-acetamide

There total 5 articles about 2-(3,4,5-trimethoxyphenyl)-2-acetoxy-N-methyl-N-(1-(3-methoxyphenyl)ethyl)-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:

: 929048-66-8
α-acetoxy-3,4,5-trimethoxyphenylacetic acid

: 438245-97-7
1-(3-methoxyphenyl)-N-methylethan-1-amine

: 929048-90-8
2-(3,4,5-trimethoxyphenyl)-2-acetoxy-N-methyl-N-(1-(3-methoxyphenyl)ethyl)-acetamide

Guidance literature:: α-acetoxy-3,4,5-trimethoxyphenylacetic acid; With 1,1'-carbonyldiimidazole; In dichloromethane; at 20 ℃; for 1h; Heating / reflux;

1-(3-methoxyphenyl)-N-methylethan-1-amine; In dichloromethane; at 20 ℃; for 2h;

Reference yield:

: 86-81-7
3,4,5-trimethoxy-benzaldehyde

: 929048-90-8
2-(3,4,5-trimethoxyphenyl)-2-acetoxy-N-methyl-N-(1-(3-methoxyphenyl)ethyl)-acetamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-benzyl-N,N,N-triethylammonium chloride / dichloromethane; water / 2 h / 0 - 20 °C

2.1: hydrogenchloride / methanol / 2.83 h / 15 - 20 °C

2.2: 2 h

3.1: 3 h / 20 °C

4.1: 1,1'-carbonyldiimidazole / dichloromethane / 1 h / 20 °C / Heating / reflux

4.2: 2 h / 20 °C

With hydrogenchloride; 1,1'-carbonyldiimidazole; N-benzyl-N,N,N-triethylammonium chloride; In methanol; dichloromethane; water;

Reference yield:

: 91958-61-1,126567-31-5,126644-21-1
acetoxy-3,4,5-trimethoxyphenylacetonitrile

: 929048-90-8
2-(3,4,5-trimethoxyphenyl)-2-acetoxy-N-methyl-N-(1-(3-methoxyphenyl)ethyl)-acetamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogenchloride / methanol / 2.83 h / 15 - 20 °C

1.2: 2 h

2.1: 3 h / 20 °C

3.1: 1,1'-carbonyldiimidazole / dichloromethane / 1 h / 20 °C / Heating / reflux

3.2: 2 h / 20 °C

With hydrogenchloride; 1,1'-carbonyldiimidazole; In methanol; dichloromethane;