N-<2-hydroxy-2-(4-methoxyphenyl)ethyl>-2-(3,4-dimethoxyphenyl)acetamide

Base Information

• Chemical Name: N-<2-hydroxy-2-(4-methoxyphenyl)ethyl>-2-(3,4-dimethoxyphenyl)acetamide
• CAS No.: 104422-01-7
• Molecular Formula: C₁₉H₂₃NO₅
• Molecular Weight: 345.395
• Mol file: 104422-01-7.mol

Synonyms:N-<2-hydroxy-2-(4-methoxyphenyl)ethyl>-2-(3,4-dimethoxyphenyl)acetamide

Chemical Property of N-<2-hydroxy-2-(4-methoxyphenyl)ethyl>-2-(3,4-dimethoxyphenyl)acetamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-<2-hydroxy-2-(4-methoxyphenyl)ethyl>-2-(3,4-dimethoxyphenyl)acetamide

There total 3 articles about N-<2-hydroxy-2-(4-methoxyphenyl)ethyl>-2-(3,4-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: 63.0%

2-amino-1-(4-methoxyphenyl)ethanol (55275-61-1) + 3,4-dimethoxyphenylacetyl chloride (10313-60-7) → N-<2-hydroxy-2-(4-methoxyphenyl)ethyl>-2-(3,4-dimethoxyphenyl)acetamide (104422-01-7)

Guidance literature:

With sodium hydroxide;

DOI:10.1021/jm00384a006

Reference yield:

4-methoxymandelonitrile (33646-40-1) → N-<2-hydroxy-2-(4-methoxyphenyl)ethyl>-2-(3,4-dimethoxyphenyl)acetamide (104422-01-7)

Guidance literature:

Multi-step reaction with 2 steps

1: 37 percent / BH₃ / tetrahydrofuran

2: 63 percent / 2.5 N aq. NaOH

With sodium hydroxide; borane; In tetrahydrofuran;

DOI:10.1021/jm00384a006

Reference yield:

(3,4-Dimethoxyphenyl)acetic acid (93-40-3) → N-<2-hydroxy-2-(4-methoxyphenyl)ethyl>-2-(3,4-dimethoxyphenyl)acetamide (104422-01-7)

Guidance literature:

Multi-step reaction with 2 steps

1: SOCl₂

2: 63 percent / 2.5 N aq. NaOH

With sodium hydroxide; thionyl chloride;

DOI:10.1021/jm00384a006

upstream raw materials:

2-amino-1-(4-methoxyphenyl)ethanol

3,4-dimethoxyphenylacetyl chloride

(3,4-Dimethoxyphenyl)acetic acid

4-methoxymandelonitrile

Downstream raw materials:

N-[2-(3,4-dimethoxyphenyl)-ethyl]-2-hydroxy-2-(4-methoxyphenyl)ethylamine

7,8-Dimethoxy-1-(4-methoxy-phenyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepine

3-Allyl-7,8-dimethoxy-1-(4-methoxy-phenyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepine

N-allyl-2,3,4,5-tetrahydro-1-(4-hydroxyphenyl)-1H-3-benzazepine-7,8-diol hydrobromide