({(R)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-[(2S,5R)-2-isopropyl-5-methyl-cyclohex-(E)-ylidene]-ethyl}-dimethyl-silanyl)-benzene

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Chemical Name:({(R)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-[(2S,5R)-2-isopropyl-5-methyl-cyclohex-(E)-ylidene]-ethyl}-dimethyl-silanyl)-benzene
CAS No.:306973-78-4
Molecular Formula:C₂₇H₄₈OSi₂
Molecular Weight:444.849
Hs Code.:

Synonyms:({(R)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-[(2S,5R)-2-isopropyl-5-methyl-cyclohex-(E)-ylidene]-ethyl}-dimethyl-silanyl)-benzene

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Chemical Property of ({(R)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-[(2S,5R)-2-isopropyl-5-methyl-cyclohex-(E)-ylidene]-ethyl}-dimethyl-silanyl)-benzene

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Technology Process of ({(R)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-[(2S,5R)-2-isopropyl-5-methyl-cyclohex-(E)-ylidene]-ethyl}-dimethyl-silanyl)-benzene

There total 4 articles about ({(R)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-[(2S,5R)-2-isopropyl-5-methyl-cyclohex-(E)-ylidene]-ethyl}-dimethyl-silanyl)-benzene 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:

: 10458-14-7,14073-97-3,17627-49-5,7786-64-3
(2R,5S)-menthone

: 306973-78-4
({(R)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-[(2S,5R)-2-isopropyl-5-methyl-cyclohex-(E)-ylidene]-ethyl}-dimethyl-silanyl)-benzene

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-BuLi / tetrahydrofuran / 1 h / -78 °C

1.2: CeCl₃ / tetrahydrofuran / 1 h / 20 °C

1.3: 78 percent / tetrahydrofuran / 4 h / -78 °C

2.1: 73 percent / Red-Al / tetrahydrofuran / 14 h / 0 °C

3.1: n-BuLi / tetrahydrofuran / 1 h / -78 °C

3.2: tetrahydrofuran / 3.5 h / -78 - 20 °C

4.1: CuI; LiI / tetrahydrofuran / 0.5 h / -30 °C

4.2: 59 percent / tetrahydrofuran / 14 h / 20 °C

With copper(l) iodide; n-butyllithium; sodium bis(2-methoxyethoxy)aluminium dihydride; lithium iodide; In tetrahydrofuran; 1.1: Metallation / 1.2: Addition / 1.3: Addition / 2.1: Reduction / 3.1: Metallation / 3.2: Etherification / 4.1: Metallation / 4.2: Addition;
DOI:10.1021/jo000810t

Reference yield:

: 76782-82-6
tert-Butyldimethyl(prop-2-ynyloxy)silane

: 306973-78-4
({(R)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-[(2S,5R)-2-isopropyl-5-methyl-cyclohex-(E)-ylidene]-ethyl}-dimethyl-silanyl)-benzene

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-BuLi / tetrahydrofuran / 1 h / -78 °C

1.2: CeCl₃ / tetrahydrofuran / 1 h / 20 °C

1.3: 78 percent / tetrahydrofuran / 4 h / -78 °C

2.1: 73 percent / Red-Al / tetrahydrofuran / 14 h / 0 °C

3.1: n-BuLi / tetrahydrofuran / 1 h / -78 °C

3.2: tetrahydrofuran / 3.5 h / -78 - 20 °C

4.1: CuI; LiI / tetrahydrofuran / 0.5 h / -30 °C

4.2: 59 percent / tetrahydrofuran / 14 h / 20 °C

With copper(l) iodide; n-butyllithium; sodium bis(2-methoxyethoxy)aluminium dihydride; lithium iodide; In tetrahydrofuran; 1.1: Metallation / 1.2: Addition / 1.3: Addition / 2.1: Reduction / 3.1: Metallation / 3.2: Etherification / 4.1: Metallation / 4.2: Addition;
DOI:10.1021/jo000810t

Reference yield:

: 750594-48-0
(1R,2S,5R)-2-i-propyl-5-methyl-1-(3-t-butyldimethylsyloxy-1-propen-1-yl)cyclohexan-1-ol

: 306973-78-4
({(R)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-[(2S,5R)-2-isopropyl-5-methyl-cyclohex-(E)-ylidene]-ethyl}-dimethyl-silanyl)-benzene

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-BuLi / tetrahydrofuran / 1 h / -78 °C

1.2: tetrahydrofuran / 3.5 h / -78 - 20 °C

2.1: CuI; LiI / tetrahydrofuran / 0.5 h / -30 °C

2.2: 59 percent / tetrahydrofuran / 14 h / 20 °C

With copper(l) iodide; n-butyllithium; lithium iodide; In tetrahydrofuran; 1.1: Metallation / 1.2: Etherification / 2.1: Metallation / 2.2: Addition;
DOI:10.1021/jo000810t