(S)-methyl 2-(2-chloro-N-(4-methoxybenzyl)acetamido)-3-methylbutanoate

Base Information

Chemical Name:(S)-methyl 2-(2-chloro-N-(4-methoxybenzyl)acetamido)-3-methylbutanoate
CAS No.:1456900-67-6
Molecular Formula:C₁₆H₂₂ClNO₄
Molecular Weight:327.808
Hs Code.:

Synonyms:(S)-methyl 2-(2-chloro-N-(4-methoxybenzyl)acetamido)-3-methylbutanoate

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Chemical Property of (S)-methyl 2-(2-chloro-N-(4-methoxybenzyl)acetamido)-3-methylbutanoate

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Technology Process of (S)-methyl 2-(2-chloro-N-(4-methoxybenzyl)acetamido)-3-methylbutanoate

There total 4 articles about (S)-methyl 2-(2-chloro-N-(4-methoxybenzyl)acetamido)-3-methylbutanoate 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: 90.0%

: (S)-methyl 2-((4-methoxybenzyl)amino)-3-methylbutanoate

: 79-04-9
chloroacetyl chloride

: 1456900-67-6
(S)-methyl 2-(2-chloro-N-(4-methoxybenzyl)acetamido)-3-methylbutanoate

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃; for 1h;
DOI:10.1080/00397911.2019.1671983

Reference yield:

: 6306-52-1
L-valine methylester hydrochloride

: 1456900-67-6
(S)-methyl 2-(2-chloro-N-(4-methoxybenzyl)acetamido)-3-methylbutanoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: pyridine / dichloromethane / 0.08 h / 0 °C

1.2: 12 h / 0 - 20 °C

2.1: triethylamine / dichloromethane / 12 h / 0 °C

With pyridine; triethylamine; In dichloromethane;
DOI:10.1007/s00726-013-1571-4

Reference yield:

: 72-18-4,25609-85-2,7004-03-7,921-10-8
L-valine

: 1456900-67-6
(S)-methyl 2-(2-chloro-N-(4-methoxybenzyl)acetamido)-3-methylbutanoate

Guidance literature:: Multi-step reaction with 3 steps

1.1: thionyl chloride / 0 °C

2.1: pyridine / dichloromethane / 0.08 h / 0 °C

2.2: 12 h / 0 - 20 °C

3.1: triethylamine / dichloromethane / 12 h / 0 °C

With pyridine; thionyl chloride; triethylamine; In dichloromethane;
DOI:10.1007/s00726-013-1571-4