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C36H70O5Si2

Base Information Edit
C<sub>36</sub>H<sub>70</sub>O<sub>5</sub>Si<sub>2</sub>

Synonyms:C36H70O5Si2

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of C36H70O5Si2 Edit
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Technology Process of C36H70O5Si2

There total 18 articles about C36H70O5Si2 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:
Guidance literature:
With acetic acid; tetramethylammonium triacetoxyborohydride; In acetonitrile; at -20 ℃; for 48h;
DOI:10.1016/j.tetlet.2011.07.105
Guidance literature:
Multi-step reaction with 11 steps
1.1: methanol; lithium borohydride / diethyl ether / 6 h / 20 °C
2.1: 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene / dichloromethane / 20 h / 20 °C
3.1: (+)-Ipc2BOMe / diethyl ether / 3 h / -78 - 20 °C
4.1: 1H-imidazole; dmap / dichloromethane / 12 h / 20 °C
5.1: ozone / dichloromethane / 1 h / -78 °C
5.2: 6 h / 20 °C
6.1: diethyl ether / 4 h / -78 °C
7.1: pyridine; Dess-Martin periodane / dichloromethane / 15 h / 20 °C
8.1: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / dichloromethane / 24 h / 40 °C
9.1: (triphenylphosphine)copper(I) hydride hexamer; phenylsilane / toluene / 24 h / 20 °C
10.1: methanol; pyridinium p-toluenesulfonate / dichloromethane / 0.5 h / 20 °C
11.1: acetic acid; tetramethylammonium triacetoxyborohydride / acetonitrile / 48 h / -20 °C
With pyridine; 1H-imidazole; tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; methanol; dmap; lithium borohydride; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; (triphenylphosphine)copper(I) hydride hexamer; [bis(acetoxy)iodo]benzene; phenylsilane; pyridinium p-toluenesulfonate; Dess-Martin periodane; ozone; acetic acid; tetramethylammonium triacetoxyborohydride; In diethyl ether; dichloromethane; toluene; acetonitrile;
DOI:10.1016/j.tetlet.2011.07.105
Guidance literature:
Multi-step reaction with 9 steps
1.1: (+)-Ipc2BOMe / diethyl ether / 3 h / -78 - 20 °C
2.1: 1H-imidazole; dmap / dichloromethane / 12 h / 20 °C
3.1: ozone / dichloromethane / 1 h / -78 °C
3.2: 6 h / 20 °C
4.1: diethyl ether / 4 h / -78 °C
5.1: pyridine; Dess-Martin periodane / dichloromethane / 15 h / 20 °C
6.1: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / dichloromethane / 24 h / 40 °C
7.1: (triphenylphosphine)copper(I) hydride hexamer; phenylsilane / toluene / 24 h / 20 °C
8.1: methanol; pyridinium p-toluenesulfonate / dichloromethane / 0.5 h / 20 °C
9.1: acetic acid; tetramethylammonium triacetoxyborohydride / acetonitrile / 48 h / -20 °C
With pyridine; 1H-imidazole; tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; methanol; dmap; (triphenylphosphine)copper(I) hydride hexamer; phenylsilane; pyridinium p-toluenesulfonate; Dess-Martin periodane; ozone; acetic acid; tetramethylammonium triacetoxyborohydride; In diethyl ether; dichloromethane; toluene; acetonitrile;
DOI:10.1016/j.tetlet.2011.07.105
upstream raw materials:

C27H50O3Si2

C21H36O3Si

C16H34OSi

C10H20O

Downstream raw materials:

C39H74O5Si2

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