1-benzyl 3-ethyl 2-((tert-butyldimethylsilyloxy)methyl)-4-(4-hydroxyphenyl)-5,6-dihydropyridine-1,3(2H)-dicarboxylate

Base Information

Chemical Name:1-benzyl 3-ethyl 2-((tert-butyldimethylsilyloxy)methyl)-4-(4-hydroxyphenyl)-5,6-dihydropyridine-1,3(2H)-dicarboxylate
CAS No.:1361293-64-2
Molecular Formula:C₂₉H₃₉NO₆Si
Molecular Weight:525.717
Hs Code.:

Synonyms:1-benzyl 3-ethyl 2-((tert-butyldimethylsilyloxy)methyl)-4-(4-hydroxyphenyl)-5,6-dihydropyridine-1,3(2H)-dicarboxylate

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Chemical Property of 1-benzyl 3-ethyl 2-((tert-butyldimethylsilyloxy)methyl)-4-(4-hydroxyphenyl)-5,6-dihydropyridine-1,3(2H)-dicarboxylate

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Technology Process of 1-benzyl 3-ethyl 2-((tert-butyldimethylsilyloxy)methyl)-4-(4-hydroxyphenyl)-5,6-dihydropyridine-1,3(2H)-dicarboxylate

There total 4 articles about 1-benzyl 3-ethyl 2-((tert-butyldimethylsilyloxy)methyl)-4-(4-hydroxyphenyl)-5,6-dihydropyridine-1,3(2H)-dicarboxylate 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:

: 37595-74-7
N,N-phenylbistrifluoromethane-sulfonimide

: 1361293-43-7
Ethyl 3-((benzyloxycarbonyl)(3-ethoxy-3-oxopropyl)amino)-4-(tert-butyldimethylsilyloxy)butanoate

: 71597-85-8
(p-hydroxyphenyl)boronic acid

: 1361293-65-3
1-benzyl 3-ethyl 6-((tert-butyldimethylsilyloxy)methyl)-4-(4-hydroxyphenyl)-5,6-dihydropyridine-1,3(2H)-dicarboxylate

: 1361293-64-2
1-benzyl 3-ethyl 2-((tert-butyldimethylsilyloxy)methyl)-4-(4-hydroxyphenyl)-5,6-dihydropyridine-1,3(2H)-dicarboxylate

Guidance literature:: Ethyl 3-((benzyloxycarbonyl)(3-ethoxy-3-oxopropyl)amino)-4-(tert-butyldimethylsilyloxy)butanoate; With sodium; In ethanol; toluene; at 20 ℃; for 48h; Inert atmosphere;

With sodium hydride; In tetrahydrofuran; at 0 ℃; for 0.5h; Inert atmosphere;

N,N-phenylbistrifluoromethane-sulfonimide; (p-hydroxyphenyl)boronic acid;

Reference yield:

: 102191-92-4
tert-butyldimethylsiloxyacetaldehyde

: 1361293-65-3
1-benzyl 3-ethyl 6-((tert-butyldimethylsilyloxy)methyl)-4-(4-hydroxyphenyl)-5,6-dihydropyridine-1,3(2H)-dicarboxylate

: 1361293-64-2
1-benzyl 3-ethyl 2-((tert-butyldimethylsilyloxy)methyl)-4-(4-hydroxyphenyl)-5,6-dihydropyridine-1,3(2H)-dicarboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: toluene / 5 h / 20 - 50 °C / Inert atmosphere

2.1: ethanol / 20 °C / Inert atmosphere; Reflux

3.1: sodium hydrogencarbonate / 1,4-dioxane / 0 - 20 °C / Inert atmosphere

4.1: sodium / toluene; ethanol / 48 h / 20 °C / Inert atmosphere

4.2: 0.5 h / 0 °C / Inert atmosphere

With sodium; sodium hydrogencarbonate; In 1,4-dioxane; ethanol; toluene;

Reference yield:

: 94844-37-8
ethyl (2E)-4-{[tert-butyl(dimethyl)silyl]oxy}but-2-enoate

: 1361293-65-3
1-benzyl 3-ethyl 6-((tert-butyldimethylsilyloxy)methyl)-4-(4-hydroxyphenyl)-5,6-dihydropyridine-1,3(2H)-dicarboxylate

: 1361293-64-2
1-benzyl 3-ethyl 2-((tert-butyldimethylsilyloxy)methyl)-4-(4-hydroxyphenyl)-5,6-dihydropyridine-1,3(2H)-dicarboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: ethanol / 20 °C / Inert atmosphere; Reflux

2.1: sodium hydrogencarbonate / 1,4-dioxane / 0 - 20 °C / Inert atmosphere

3.1: sodium / toluene; ethanol / 48 h / 20 °C / Inert atmosphere

3.2: 0.5 h / 0 °C / Inert atmosphere

With sodium; sodium hydrogencarbonate; In 1,4-dioxane; ethanol; toluene;