dimethyl 2-(4-((tert-butyldimethylsilyl)oxy)benzyl)-3-(cis-4-((tert-butyldimethylsilyl)oxy)cyclohexyl)maleate

Base Information

Chemical Name:dimethyl 2-(4-((tert-butyldimethylsilyl)oxy)benzyl)-3-(cis-4-((tert-butyldimethylsilyl)oxy)cyclohexyl)maleate
CAS No.:1420039-66-2
Molecular Formula:C₃₁H₅₂O₆Si₂
Molecular Weight:576.921
Hs Code.:

Synonyms:dimethyl 2-(4-((tert-butyldimethylsilyl)oxy)benzyl)-3-(cis-4-((tert-butyldimethylsilyl)oxy)cyclohexyl)maleate

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Chemical Property of dimethyl 2-(4-((tert-butyldimethylsilyl)oxy)benzyl)-3-(cis-4-((tert-butyldimethylsilyl)oxy)cyclohexyl)maleate

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Technology Process of dimethyl 2-(4-((tert-butyldimethylsilyl)oxy)benzyl)-3-(cis-4-((tert-butyldimethylsilyl)oxy)cyclohexyl)maleate

There total 14 articles about dimethyl 2-(4-((tert-butyldimethylsilyl)oxy)benzyl)-3-(cis-4-((tert-butyldimethylsilyl)oxy)cyclohexyl)maleate 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: 85.0%

: 1420039-64-0
3-(4-((tert-butyldimethylsilyl)oxy)benzyl)-4-(cis-4-((tert-butyldimethylsilyl)oxy)cyclohexyl)furan-2,5-dione

: 18107-18-1
diazomethyl-trimethyl-silane

: 1420039-66-2
dimethyl 2-(4-((tert-butyldimethylsilyl)oxy)benzyl)-3-(cis-4-((tert-butyldimethylsilyl)oxy)cyclohexyl)maleate

Guidance literature:: In methanol; diethyl ether; at 20 ℃; for 5h;

Reference yield:

: 31770-76-0
3-(4-hydroxyphenyl)propionic acid benzyl ester

: 1420039-66-2
dimethyl 2-(4-((tert-butyldimethylsilyl)oxy)benzyl)-3-(cis-4-((tert-butyldimethylsilyl)oxy)cyclohexyl)maleate

Guidance literature:: Multi-step reaction with 5 steps

1.1: 1H-imidazole / dichloromethane / 15 h / 0 - 20 °C

2.1: n-butyllithium; diisopropylamine / tetrahydrofuran; hexane / 1.5 h / -78 - 0 °C / Inert atmosphere

2.2: 1 h / -78 °C

3.1: palladium 10% on activated carbon; hydrogen / 24 h / Inert atmosphere

4.1: acetic anhydride / 18 h / 120 °C

5.1: methanol; diethyl ether / 5 h / 20 °C

With 1H-imidazole; n-butyllithium; palladium 10% on activated carbon; hydrogen; acetic anhydride; diisopropylamine; In tetrahydrofuran; methanol; diethyl ether; hexane; dichloromethane;

Reference yield:

: 929556-81-0
benzyl 3-(4-((tert-butyldimethylsilyl)oxy)phenyl)propanoate

: 1420039-66-2
dimethyl 2-(4-((tert-butyldimethylsilyl)oxy)benzyl)-3-(cis-4-((tert-butyldimethylsilyl)oxy)cyclohexyl)maleate

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-butyllithium; diisopropylamine / tetrahydrofuran; hexane / 1.5 h / -78 - 0 °C / Inert atmosphere

1.2: 1 h / -78 °C

2.1: palladium 10% on activated carbon; hydrogen / 24 h / Inert atmosphere

3.1: acetic anhydride / 18 h / 120 °C

4.1: methanol; diethyl ether / 5 h / 20 °C

With n-butyllithium; palladium 10% on activated carbon; hydrogen; acetic anhydride; diisopropylamine; In tetrahydrofuran; methanol; diethyl ether; hexane;