(S)-3-(2-triisopropylsilyloxyethyl)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-enone

Base Information

Chemical Name:(S)-3-(2-triisopropylsilyloxyethyl)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-enone
CAS No.:1359761-48-0
Molecular Formula:C₂₁H₃₈O₂Si
Molecular Weight:350.617
Hs Code.:

Synonyms:(S)-3-(2-triisopropylsilyloxyethyl)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-enone

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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 (S)-3-(2-triisopropylsilyloxyethyl)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-enone

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Technology Process of (S)-3-(2-triisopropylsilyloxyethyl)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-enone

There total 4 articles about (S)-3-(2-triisopropylsilyloxyethyl)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-enone 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: 86.0%

: 1359761-47-9
(1S,5R)-1-(2-triisopropylsilyloxyethyl)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-enol

: 1359761-48-0
(S)-3-(2-triisopropylsilyloxyethyl)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-enone

Guidance literature:: With pyridinium chlorochromate; In dichloromethane; at 23 ℃; for 54h;
DOI:10.1021/ol300058t

Reference yield:

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

: 1359761-48-0
(S)-3-(2-triisopropylsilyloxyethyl)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-enone

Guidance literature:: Multi-step reaction with 4 steps

1.1: lithium diisopropyl amide / tetrahydrofuran / 1.17 h / -78 °C

1.2: 2 h / -78 °C

2.1: lithium aluminium tetrahydride / diethyl ether / 2 h / 20 °C

3.1: 1H-imidazole / N,N-dimethyl-formamide / 14 h / 20 °C

4.1: pyridinium chlorochromate / dichloromethane / 54 h / 23 °C

With 1H-imidazole; lithium aluminium tetrahydride; pyridinium chlorochromate; lithium diisopropyl amide; In tetrahydrofuran; diethyl ether; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ol300058t

Reference yield:

: 773889-84-2
(1S,5R)-1-(2-hydroxyethyl)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-enol

: 1359761-48-0
(S)-3-(2-triisopropylsilyloxyethyl)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-enone

Guidance literature:: Multi-step reaction with 2 steps

1: 1H-imidazole / N,N-dimethyl-formamide / 14 h / 20 °C

2: pyridinium chlorochromate / dichloromethane / 54 h / 23 °C

With 1H-imidazole; pyridinium chlorochromate; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ol300058t