ethyl 3-cyclohexylidene-2-{[(trimethylsilyl)oxy]sulfonyl}prop-2-enoate

Base Information

Chemical Name:ethyl 3-cyclohexylidene-2-{[(trimethylsilyl)oxy]sulfonyl}prop-2-enoate
CAS No.:1448247-80-0
Molecular Formula:C₁₄H₂₄O₅SSi
Molecular Weight:332.493
Hs Code.:

Synonyms:ethyl 3-cyclohexylidene-2-{[(trimethylsilyl)oxy]sulfonyl}prop-2-enoate

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Chemical Property of ethyl 3-cyclohexylidene-2-{[(trimethylsilyl)oxy]sulfonyl}prop-2-enoate

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Technology Process of ethyl 3-cyclohexylidene-2-{[(trimethylsilyl)oxy]sulfonyl}prop-2-enoate

There total 2 articles about ethyl 3-cyclohexylidene-2-{[(trimethylsilyl)oxy]sulfonyl}prop-2-enoate 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: 62.0%

: 4353-77-9
chlorosulfonate de trimethylsilyle

: 156861-44-8
ethyl 3-cyclohexyliden-2-propenoate

: 1448247-80-0
ethyl 3-cyclohexylidene-2-{[(trimethylsilyl)oxy]sulfonyl}prop-2-enoate

Guidance literature:: ethyl 3-cyclohexyliden-2-propenoate; With n-butyllithium; In tetrahydrofuran; hexane; at -60 ℃; for 1h; Inert atmosphere;

chlorosulfonate de trimethylsilyle; In tetrahydrofuran; hexane; at -60 - 20 ℃; for 2h; Inert atmosphere;
DOI:10.1080/10426507.2012.718299

Reference yield:

: 5664-20-0
vinylidenecyclohexane

: 1448247-80-0
ethyl 3-cyclohexylidene-2-{[(trimethylsilyl)oxy]sulfonyl}prop-2-enoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-butyllithium / tetrahydrofuran / 2 h / -60 - -20 °C / Inert atmosphere

1.2: 1 h / -60 - 20 °C / Inert atmosphere

2.1: n-butyllithium / tetrahydrofuran; hexane / 1 h / -60 °C / Inert atmosphere

2.2: 2 h / -60 - 20 °C / Inert atmosphere

With n-butyllithium; In tetrahydrofuran; hexane;
DOI:10.1080/10426507.2012.718299