ethyl 4-oxo-1-(((2-(trimethylsilyl)ethoxy)methoxy)methyl)cyclohex-2-enecarboxylate

Base Information

Chemical Name:ethyl 4-oxo-1-(((2-(trimethylsilyl)ethoxy)methoxy)methyl)cyclohex-2-enecarboxylate
CAS No.:1422463-69-1
Molecular Formula:C₁₆H₂₈O₅Si
Molecular Weight:328.481
Hs Code.:

Synonyms:ethyl 4-oxo-1-(((2-(trimethylsilyl)ethoxy)methoxy)methyl)cyclohex-2-enecarboxylate

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Chemical Property of ethyl 4-oxo-1-(((2-(trimethylsilyl)ethoxy)methoxy)methyl)cyclohex-2-enecarboxylate

Chemical Property:

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Technology Process of ethyl 4-oxo-1-(((2-(trimethylsilyl)ethoxy)methoxy)methyl)cyclohex-2-enecarboxylate

There total 4 articles about ethyl 4-oxo-1-(((2-(trimethylsilyl)ethoxy)methoxy)methyl)cyclohex-2-enecarboxylate 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:

: C₂₀H₄₀O₆Si₂

: 1422463-69-1
ethyl 4-oxo-1-(((2-(trimethylsilyl)ethoxy)methoxy)methyl)cyclohex-2-enecarboxylate

Guidance literature:: With pyridinium p-toluenesulfonate; In tetrahydrofuran; at 60 ℃; for 2h; Solvent; Temperature; Inert atmosphere;
DOI:10.1016/j.tet.2012.12.079

Reference yield:

: 10029-04-6
ethyl 2-(hydroxymethyl)acrylate

: 1422463-69-1
ethyl 4-oxo-1-(((2-(trimethylsilyl)ethoxy)methoxy)methyl)cyclohex-2-enecarboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / Inert atmosphere; Cooling with ice

2: neat (no solvent) / 1 h / 150 °C / Inert atmosphere; Microwave irradiation

3: pyridinium p-toluenesulfonate / tetrahydrofuran / 2 h / 60 °C / Inert atmosphere

With pyridinium p-toluenesulfonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; 2: |Diels-Alder Cycloaddition;
DOI:10.1016/j.tet.2012.12.079

Reference yield:

: 76513-69-4
(2-trimethylethylsilylethoxy)methyl chloride

: 1422463-69-1
ethyl 4-oxo-1-(((2-(trimethylsilyl)ethoxy)methoxy)methyl)cyclohex-2-enecarboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / Inert atmosphere; Cooling with ice

2: neat (no solvent) / 1 h / 150 °C / Inert atmosphere; Microwave irradiation

3: pyridinium p-toluenesulfonate / tetrahydrofuran / 2 h / 60 °C / Inert atmosphere

With pyridinium p-toluenesulfonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; 2: |Diels-Alder Cycloaddition;
DOI:10.1016/j.tet.2012.12.079