methyl (+/-)-3-carbomethoxy-4-[2-(methylamino)methyl-4-methoxyphenyl]butanoate

Base Information

Chemical Name:methyl (+/-)-3-carbomethoxy-4-[2-(methylamino)methyl-4-methoxyphenyl]butanoate
CAS No.:205676-69-3
Molecular Formula:C₁₆H₂₃NO₅
Molecular Weight:309.362
Hs Code.:

Synonyms:methyl (+/-)-3-carbomethoxy-4-[2-(methylamino)methyl-4-methoxyphenyl]butanoate

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Chemical Property of methyl (+/-)-3-carbomethoxy-4-[2-(methylamino)methyl-4-methoxyphenyl]butanoate

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Technology Process of methyl (+/-)-3-carbomethoxy-4-[2-(methylamino)methyl-4-methoxyphenyl]butanoate

There total 6 articles about methyl (+/-)-3-carbomethoxy-4-[2-(methylamino)methyl-4-methoxyphenyl]butanoate 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: 100.0%

: 205676-68-2
Methyl (+/-)-3-carbomethoxy-4-[2-[N-(tert-butoxycarbonyl)-N-methylamino]methyl-4-methoxyphenyl]butanoate

: 205676-69-3
methyl (+/-)-3-carbomethoxy-4-[2-(methylamino)methyl-4-methoxyphenyl]butanoate

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 0 - 20 ℃; for 1h;

Reference yield:

: C₂₁H₂₉NO₇

: 205676-69-3
methyl (+/-)-3-carbomethoxy-4-[2-(methylamino)methyl-4-methoxyphenyl]butanoate

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen / palladium 10% on activated carbon / methanol / 5 h / 2585.81 Torr

2: trifluoroacetic acid / dichloromethane / 1 h / 0 - 20 °C

With hydrogen; trifluoroacetic acid; palladium 10% on activated carbon; In methanol; dichloromethane;

Reference yield:

: 19614-12-1
2-bromo-5-methoxybenzyl bromide

: 205676-69-3
methyl (+/-)-3-carbomethoxy-4-[2-(methylamino)methyl-4-methoxyphenyl]butanoate

Guidance literature:: Multi-step reaction with 5 steps

1: tetrahydrofuran; water / 2.5 h / 20 °C

2: chloroform / 0.75 h / 20 °C

3: N-ethyl-N,N-diisopropylamine / palladium diacetate; tris-(o-tolyl)phosphine / propiononitrile / 0.75 h / Heating / reflux

4: hydrogen / palladium 10% on activated carbon / methanol / 5 h / 2585.81 Torr

5: trifluoroacetic acid / dichloromethane / 1 h / 0 - 20 °C

With hydrogen; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; palladium diacetate; palladium 10% on activated carbon; tris-(o-tolyl)phosphine; In tetrahydrofuran; methanol; dichloromethane; chloroform; water; propiononitrile;