(5R)-2-methyl-5-(prop-1-en-2-yl)-1-(((triisopropylsilyl)oxy)methyl)cyclohex-2-enol

Base Information

Chemical Name:(5R)-2-methyl-5-(prop-1-en-2-yl)-1-(((triisopropylsilyl)oxy)methyl)cyclohex-2-enol
CAS No.:1359761-40-2
Molecular Formula:C₂₀H₃₈O₂Si
Molecular Weight:338.606
Hs Code.:

Synonyms:(5R)-2-methyl-5-(prop-1-en-2-yl)-1-(((triisopropylsilyl)oxy)methyl)cyclohex-2-enol

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (5R)-2-methyl-5-(prop-1-en-2-yl)-1-(((triisopropylsilyl)oxy)methyl)cyclohex-2-enol

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Technology Process of (5R)-2-methyl-5-(prop-1-en-2-yl)-1-(((triisopropylsilyl)oxy)methyl)cyclohex-2-enol

There total 3 articles about (5R)-2-methyl-5-(prop-1-en-2-yl)-1-(((triisopropylsilyl)oxy)methyl)cyclohex-2-enol 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: 93.0%

: trans-(5R)-1-(hydroxymethyl)-5-isopropenyl-2-methylcyclohex-2-ene-1-ol

: 13154-24-0
triisopropylsilyl chloride

: 1359761-40-2
(5R)-2-methyl-5-(prop-1-en-2-yl)-1-(((triisopropylsilyl)oxy)methyl)cyclohex-2-enol

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; at 20 ℃; for 24h; Inert atmosphere;
DOI:10.1021/ol300058t

Reference yield:

: (5R)-1-(chlormethyl)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-enol

: 1359761-40-2
(5R)-2-methyl-5-(prop-1-en-2-yl)-1-(((triisopropylsilyl)oxy)methyl)cyclohex-2-enol

Guidance literature:: Multi-step reaction with 2 steps

1: water; potassium hydroxide / 1,4-dioxane / 6 h / 20 - 75 °C

2: 1H-imidazole / N,N-dimethyl-formamide / 24 h / 20 °C / Inert atmosphere

With 1H-imidazole; water; potassium hydroxide; In 1,4-dioxane; N,N-dimethyl-formamide;
DOI:10.1021/ol300058t

Reference yield:

: 6485-40-1,2244-16-8
(R)-Carvone

: 1359761-40-2
(5R)-2-methyl-5-(prop-1-en-2-yl)-1-(((triisopropylsilyl)oxy)methyl)cyclohex-2-enol

Guidance literature:: Multi-step reaction with 3 steps

1: methyllithium lithium bromide / tetrahydrofuran; diethyl ether / 0.45 h / -78 °C / Inert atmosphere

2: water; potassium hydroxide / 1,4-dioxane / 6 h / 20 - 75 °C

3: 1H-imidazole / N,N-dimethyl-formamide / 24 h / 20 °C / Inert atmosphere

With 1H-imidazole; methyllithium lithium bromide; water; potassium hydroxide; In tetrahydrofuran; 1,4-dioxane; diethyl ether; N,N-dimethyl-formamide;
DOI:10.1021/ol300058t