methyl 2,6-dimethyl-6-<(E)-2-(trimethylsilyl)vinyl>-1-cyclohexene-1-carboxylate

Base Information

Chemical Name:methyl 2,6-dimethyl-6-<(E)-2-(trimethylsilyl)vinyl>-1-cyclohexene-1-carboxylate
CAS No.:98127-03-8
Molecular Formula:C₁₅H₂₆O₂Si
Molecular Weight:266.456
Hs Code.:

Synonyms:methyl 2,6-dimethyl-6-<(E)-2-(trimethylsilyl)vinyl>-1-cyclohexene-1-carboxylate

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Chemical Property of methyl 2,6-dimethyl-6-<(E)-2-(trimethylsilyl)vinyl>-1-cyclohexene-1-carboxylate

Chemical Property:

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Technology Process of methyl 2,6-dimethyl-6-<(E)-2-(trimethylsilyl)vinyl>-1-cyclohexene-1-carboxylate

There total 5 articles about methyl 2,6-dimethyl-6-<(E)-2-(trimethylsilyl)vinyl>-1-cyclohexene-1-carboxylate 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:

: 41309-43-7
(2-bromovinyl)trimethylsilane

: 98127-03-8
methyl 2,6-dimethyl-6-<(E)-2-(trimethylsilyl)vinyl>-1-cyclohexene-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) t-butyllithium, 2.) CuI

2: 1.) NaH / 1.) ether, 10 min, 2.) ether, 2 h

3: 1.) CuI / 1.) ether, -20 deg C, 2.) ether, -20 deg C, 3 h

With copper(l) iodide; tert.-butyl lithium; sodium hydride;
DOI:10.1021/jo00221a027

Reference yield:

: 3128-06-1
5-ketohexanoic acid

: 98127-03-8
methyl 2,6-dimethyl-6-<(E)-2-(trimethylsilyl)vinyl>-1-cyclohexene-1-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1: 80 percent / SOCl₂ / benzene / 10 h / Heating

2: 1.) lithium diisopropylamide / 1.) THF, -78 deg C, 0.5 h, 2.) THF, a) -78 deg C, 4 h, b) 25 deg C, 8 h

3: 1.) t-butyllithium, 2.) CuI

4: 1.) NaH / 1.) ether, 10 min, 2.) ether, 2 h

5: 1.) CuI / 1.) ether, -20 deg C, 2.) ether, -20 deg C, 3 h

With copper(l) iodide; thionyl chloride; tert.-butyl lithium; sodium hydride; lithium diisopropyl amide; In benzene;
DOI:10.1021/jo00221a027

Reference yield:

: 86891-79-4
methyl 3-methyl-1-oxo-2-cyclohexene-2-carboxylate

: 98127-03-8
methyl 2,6-dimethyl-6-<(E)-2-(trimethylsilyl)vinyl>-1-cyclohexene-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) t-butyllithium, 2.) CuI

2: 1.) NaH / 1.) ether, 10 min, 2.) ether, 2 h

3: 1.) CuI / 1.) ether, -20 deg C, 2.) ether, -20 deg C, 3 h

With copper(l) iodide; tert.-butyl lithium; sodium hydride;
DOI:10.1021/jo00221a027