methyl (3S)-3-[(1R)-N-(4-methoxybenzyl)-1-(4-methoxyphenyl)ethylamino]-3-phenylpropanoate

Base Information

• Chemical Name: methyl (3S)-3-[(1R)-N-(4-methoxybenzyl)-1-(4-methoxyphenyl)ethylamino]-3-phenylpropanoate
• CAS No.: 281664-28-6
• Molecular Formula: C₂₇H₃₁NO₄
• Molecular Weight: 433.547
• Mol file: 281664-28-6.mol

Synonyms:methyl (3S)-3-[(1R)-N-(4-methoxybenzyl)-1-(4-methoxyphenyl)ethylamino]-3-phenylpropanoate

Chemical Property of methyl (3S)-3-[(1R)-N-(4-methoxybenzyl)-1-(4-methoxyphenyl)ethylamino]-3-phenylpropanoate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of methyl (3S)-3-[(1R)-N-(4-methoxybenzyl)-1-(4-methoxyphenyl)ethylamino]-3-phenylpropanoate

There total 3 articles about methyl (3S)-3-[(1R)-N-(4-methoxybenzyl)-1-(4-methoxyphenyl)ethylamino]-3-phenylpropanoate 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: 44.0%

Methyl cinnamate (103-26-4,1754-62-7) + (R)-(+)-N-4-Methoxybenzyl-1-(4-methoxyphenyl)ethylamine (281664-25-3) → methyl (3S)-3-[(1R)-N-(4-methoxybenzyl)-1-(4-methoxyphenyl)ethylamino]-3-phenylpropanoate (281664-28-6)

Guidance literature:

With n-butyllithium; In tetrahydrofuran; at -78 ℃;

DOI:10.1080/00397910008087223

Reference yield:

1(R)-(4-methoxyphenyl)-ethylamine (6298-96-0,22038-86-4,35600-82-9,41851-59-6) → methyl (3S)-3-[(1R)-N-(4-methoxybenzyl)-1-(4-methoxyphenyl)ethylamino]-3-phenylpropanoate (281664-28-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 77 percent / potassium carbonate / various solvent(s) / 65 °C

2: 44 percent / n-BuLi / tetrahydrofuran / -78 °C

With n-butyllithium; potassium carbonate; In tetrahydrofuran; 2: Michael addition;

DOI:10.1080/00397910008087223

Reference yield:

p-Methoxybenzyl bromide (2746-25-0) → methyl (3S)-3-[(1R)-N-(4-methoxybenzyl)-1-(4-methoxyphenyl)ethylamino]-3-phenylpropanoate (281664-28-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 77 percent / potassium carbonate / various solvent(s) / 65 °C

2: 44 percent / n-BuLi / tetrahydrofuran / -78 °C

With n-butyllithium; potassium carbonate; In tetrahydrofuran; 2: Michael addition;

DOI:10.1080/00397910008087223

upstream raw materials:

Methyl cinnamate

(R)-(+)-N-4-Methoxybenzyl-1-(4-methoxyphenyl)ethylamine

1(R)-(4-methoxyphenyl)-ethylamine

p-Methoxybenzyl bromide

Downstream raw materials:

(3S)-methyl 3-amino-3-phenylpropanoate