methyl 2-(2,4-dimethoxyphenyl)-3-(4-methoxy-2-O-methoxymethylphenyl)propanoate

Base Information

Chemical Name:methyl 2-(2,4-dimethoxyphenyl)-3-(4-methoxy-2-O-methoxymethylphenyl)propanoate
CAS No.:213970-33-3
Molecular Formula:C₂₁H₂₆O₇
Molecular Weight:390.433
Hs Code.:

Synonyms:methyl 2-(2,4-dimethoxyphenyl)-3-(4-methoxy-2-O-methoxymethylphenyl)propanoate

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Chemical Property of methyl 2-(2,4-dimethoxyphenyl)-3-(4-methoxy-2-O-methoxymethylphenyl)propanoate

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Technology Process of methyl 2-(2,4-dimethoxyphenyl)-3-(4-methoxy-2-O-methoxymethylphenyl)propanoate

There total 4 articles about methyl 2-(2,4-dimethoxyphenyl)-3-(4-methoxy-2-O-methoxymethylphenyl)propanoate 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: 42.0%

: 55954-25-1
methyl 2-(2,4-dimethoxyphenyl)acetate

: 152955-15-2
4-methoxy-2-O-methoxymethylbenzyl bromide

: 213970-33-3
methyl 2-(2,4-dimethoxyphenyl)-3-(4-methoxy-2-O-methoxymethylphenyl)propanoate

Guidance literature:: With N,N,N,N,N,N-hexamethylphosphoric triamide; n-butyllithium; N-cyclohexylisopropylamine; In tetrahydrofuran; hexane; at -78 ℃; for 0.5h;
DOI:10.3987/com-98-8149

Reference yield:

: 673-22-3
2-Hydroxy-4-methoxybenzaldehyde

: 213970-33-3
methyl 2-(2,4-dimethoxyphenyl)-3-(4-methoxy-2-O-methoxymethylphenyl)propanoate

Guidance literature:: Multi-step reaction with 4 steps

1: 89 percent / NaH / dimethylformamide / Ambient temperature

2: 96 percent / NaBH₄ / tetrahydrofuran; ethanol / 0.75 h / Ambient temperature

3: 70 percent / LiBr, 2,6-lutidine, methanesulfonic anhydride / tetrahydrofuran / 30 h / Ambient temperature

4: 42 percent / n-BuLi, isopropylcyclohexylamine, HMPA / tetrahydrofuran; hexane / 0.5 h / -78 °C

With 2,6-dimethylpyridine; N,N,N,N,N,N-hexamethylphosphoric triamide; sodium tetrahydroborate; n-butyllithium; N-cyclohexylisopropylamine; sodium hydride; lithium bromide; Methanesulfonic anhydride; In tetrahydrofuran; ethanol; hexane; N,N-dimethyl-formamide;
DOI:10.3987/com-98-8149

Reference yield:

: 124555-63-1
4-methoxy-2-methoxymethoxy benzaldehyde

: 213970-33-3
methyl 2-(2,4-dimethoxyphenyl)-3-(4-methoxy-2-O-methoxymethylphenyl)propanoate

Guidance literature:: Multi-step reaction with 3 steps

1: 96 percent / NaBH₄ / tetrahydrofuran; ethanol / 0.75 h / Ambient temperature

2: 70 percent / LiBr, 2,6-lutidine, methanesulfonic anhydride / tetrahydrofuran / 30 h / Ambient temperature

3: 42 percent / n-BuLi, isopropylcyclohexylamine, HMPA / tetrahydrofuran; hexane / 0.5 h / -78 °C

With 2,6-dimethylpyridine; N,N,N,N,N,N-hexamethylphosphoric triamide; sodium tetrahydroborate; n-butyllithium; N-cyclohexylisopropylamine; lithium bromide; Methanesulfonic anhydride; In tetrahydrofuran; ethanol; hexane;
DOI:10.3987/com-98-8149