(2R,7Z)-9-(tert-Butyldiphenylsilyloxy)-2-methyl-1-(p-tolylsulfonyloxy)non-7-ene

Base Information

Chemical Name:(2R,7Z)-9-(tert-Butyldiphenylsilyloxy)-2-methyl-1-(p-tolylsulfonyloxy)non-7-ene
CAS No.:247166-64-9
Molecular Formula:C₃₃H₄₄O₄SSi
Molecular Weight:564.861
Hs Code.:

Synonyms:(2R,7Z)-9-(tert-Butyldiphenylsilyloxy)-2-methyl-1-(p-tolylsulfonyloxy)non-7-ene

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Chemical Property of (2R,7Z)-9-(tert-Butyldiphenylsilyloxy)-2-methyl-1-(p-tolylsulfonyloxy)non-7-ene

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Technology Process of (2R,7Z)-9-(tert-Butyldiphenylsilyloxy)-2-methyl-1-(p-tolylsulfonyloxy)non-7-ene

There total 6 articles about (2R,7Z)-9-(tert-Butyldiphenylsilyloxy)-2-methyl-1-(p-tolylsulfonyloxy)non-7-ene 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: 100.0%

: 98-59-9
p-toluenesulfonyl chloride

: 247166-63-8
(2R,7Z)-9-(tert-Butyldiphenylsilyloxy)-2-methylnon-7-en-1-ol

: 247166-64-9
(2R,7Z)-9-(tert-Butyldiphenylsilyloxy)-2-methyl-1-(p-tolylsulfonyloxy)non-7-ene

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃;

Reference yield:

: 247166-58-1
(7R)-7-Methyl-8-(tetrahydro-2H-pyran-2-yloxy)oct-1-ene

: 247166-64-9
(2R,7Z)-9-(tert-Butyldiphenylsilyloxy)-2-methyl-1-(p-tolylsulfonyloxy)non-7-ene

Guidance literature:: Multi-step reaction with 6 steps

1.1: O₃ / CH₂Cl₂ / -78 - 0 °C

1.2: 78 percent / PPh₃ / CH₂Cl₂ / 0 - 20 °C

2.1: 89 percent / 18-Crown-6; KHMDS / tetrahydrofuran; toluene / -78 - 20 °C

3.1: 100 percent / DIBAL-H / tetrahydrofuran; toluene / -78 °C

4.1: 87 percent / Et₃N / CH₂Cl₂ / 72 h

5.1: 75 percent / AcOH; Water / tetrahydrofuran / 36 h / 45 °C

6.1: 100 percent / Et₃N / CH₂Cl₂ / 20 °C

With 18-crown-6 ether; water; potassium hexamethylsilazane; diisobutylaluminium hydride; ozone; acetic acid; triethylamine; In tetrahydrofuran; dichloromethane; toluene; 1.1: Oxidation / 1.2: Reduction / 2.1: Condensation / 3.1: Reduction / 4.1: Substitution / 5.1: Hydrolysis / 6.1: Tosylation;

Reference yield:

: 247166-59-2
(6R)-6-Methyl-7-(tetrahydro-2H-pyran-2-yloxy)heptanal

: 247166-64-9
(2R,7Z)-9-(tert-Butyldiphenylsilyloxy)-2-methyl-1-(p-tolylsulfonyloxy)non-7-ene

Guidance literature:: Multi-step reaction with 5 steps

1: 89 percent / 18-Crown-6; KHMDS / tetrahydrofuran; toluene / -78 - 20 °C

2: 100 percent / DIBAL-H / tetrahydrofuran; toluene / -78 °C

3: 87 percent / Et₃N / CH₂Cl₂ / 72 h

4: 75 percent / AcOH; Water / tetrahydrofuran / 36 h / 45 °C

5: 100 percent / Et₃N / CH₂Cl₂ / 20 °C

With 18-crown-6 ether; water; potassium hexamethylsilazane; diisobutylaluminium hydride; acetic acid; triethylamine; In tetrahydrofuran; dichloromethane; toluene; 1: Condensation / 2: Reduction / 3: Substitution / 4: Hydrolysis / 5: Tosylation;