tert-butyl-diphenyl-[3-(tetrahydro-pyran-2-yloxy)-tridec-12-enyloxy]-silane

Base Information

Chemical Name:tert-butyl-diphenyl-[3-(tetrahydro-pyran-2-yloxy)-tridec-12-enyloxy]-silane
CAS No.:532929-57-0
Molecular Formula:C₃₄H₅₂O₃Si
Molecular Weight:536.871
Hs Code.:

<i>tert</i>-butyl-diphenyl-[3-(tetrahydro-pyran-2-yloxy)-tridec-12-enyloxy]-silane

Synonyms:tert-butyl-diphenyl-[3-(tetrahydro-pyran-2-yloxy)-tridec-12-enyloxy]-silane

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Chemical Property of tert-butyl-diphenyl-[3-(tetrahydro-pyran-2-yloxy)-tridec-12-enyloxy]-silane

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Technology Process of tert-butyl-diphenyl-[3-(tetrahydro-pyran-2-yloxy)-tridec-12-enyloxy]-silane

There total 5 articles about tert-butyl-diphenyl-[3-(tetrahydro-pyran-2-yloxy)-tridec-12-enyloxy]-silane 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: 99.0%

: 110-87-2
3,4-dihydro-2H-pyran

: 532929-17-2
1-(tert-butyl-diphenyl-silanyloxy)-tridec-12-en-3-ol

: 532929-57-0
tert-butyl-diphenyl-[3-(tetrahydro-pyran-2-yloxy)-tridec-12-enyloxy]-silane

Guidance literature:: With pyridinium p-toluenesulfonate; In dichloromethane; at 20 ℃;
DOI:10.1021/ol034338k

Reference yield:

: 112-45-8
10-Undecenal

: 532929-57-0
tert-butyl-diphenyl-[3-(tetrahydro-pyran-2-yloxy)-tridec-12-enyloxy]-silane

Guidance literature:: Multi-step reaction with 6 steps

1.1: NaH / tetrahydrofuran / 0 °C

2.1: i-Bu₂AlH / CH₂Cl₂ / -78 °C

3.1: 82 percent / (-)-diethyl tartrate; titanium(IV) isopropoxide; t-butyl hydroperoxide / molecular sieves 4 Angstroem / CH₂Cl₂ / -23 °C

4.1: Red-Al / tetrahydrofuran / 0 - 20 °C

4.2: 76 percent / NaIO₄ / CH₂Cl₂; acetone; H₂O

5.1: 99 percent / imidazole / dimethylformamide / 0 °C

6.1: 99 percent / pyridinium p-toluenesulfonate / CH₂Cl₂ / 20 °C

With 1H-imidazole; titanium(IV) isopropylate; tert.-butylhydroperoxide; pyridinium p-toluenesulfonate; sodium hydride; diisobutylaluminium hydride; (-)-diethyl tartrate; sodium bis(2-methoxyethoxy)aluminium dihydride; 4 A molecular sieve; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; 1.1: Wittig reaction / 3.1: Sharpless epoxidation;
DOI:10.1021/ol034338k

Reference yield:

: 148118-58-5
ethyl (E)-trideca-2,12-dienoate

: 532929-57-0
tert-butyl-diphenyl-[3-(tetrahydro-pyran-2-yloxy)-tridec-12-enyloxy]-silane

Guidance literature:: Multi-step reaction with 5 steps

1.1: i-Bu₂AlH / CH₂Cl₂ / -78 °C

2.1: 82 percent / (-)-diethyl tartrate; titanium(IV) isopropoxide; t-butyl hydroperoxide / molecular sieves 4 Angstroem / CH₂Cl₂ / -23 °C

3.1: Red-Al / tetrahydrofuran / 0 - 20 °C

3.2: 76 percent / NaIO₄ / CH₂Cl₂; acetone; H₂O

4.1: 99 percent / imidazole / dimethylformamide / 0 °C

5.1: 99 percent / pyridinium p-toluenesulfonate / CH₂Cl₂ / 20 °C

With 1H-imidazole; titanium(IV) isopropylate; tert.-butylhydroperoxide; pyridinium p-toluenesulfonate; diisobutylaluminium hydride; (-)-diethyl tartrate; sodium bis(2-methoxyethoxy)aluminium dihydride; 4 A molecular sieve; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; 2.1: Sharpless epoxidation;
DOI:10.1021/ol034338k