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C69H96O9Si3

Base Information
  • Chemical Name:C69H96O9Si3
  • CAS No.:1261152-32-2
  • Molecular Formula:C69H96O9Si3
  • Molecular Weight:1153.77
  • Hs Code.:
C<sub>69</sub>H<sub>96</sub>O<sub>9</sub>Si<sub>3</sub>

Synonyms:C69H96O9Si3

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Chemical Property of C69H96O9Si3
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Technology Process of C69H96O9Si3

There total 27 articles about C69H96O9Si3 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 N,N,N,N,-tetramethylethylenediamine; titanium tetrachloride; In tetrahydrofuran; dichloromethane; at 0 - 25 ℃; Inert atmosphere;
With lead(II) chloride; zinc; In tetrahydrofuran; dichloromethane; at 25 ℃; for 0.666667h; Inert atmosphere;
1,1-Dibromoethane; C71H100O10Si3; Further stages;
DOI:10.1021/ja109533y
Guidance literature:
With N,N,N,N,-tetramethylethylenediamine; titanium tetrachloride; In tetrahydrofuran; dichloromethane; at 0 - 25 ℃; Inert atmosphere;
With lead(II) chloride; zinc; In tetrahydrofuran; dichloromethane; at 25 ℃; for 0.666667h; Inert atmosphere;
1,1-Dibromoethane; C71H100O10Si3; Further stages;
DOI:10.1021/ja109533y
Guidance literature:
Multi-step reaction with 16 steps
1.1: 2,6-dimethylpyridine / dichloromethane / 14 h / 0 °C / Inert atmosphere
2.1: diisobutylaluminium hydride / dichloromethane / 1 h / -78 °C / Inert atmosphere
2.2: 16 h / 25 °C / Inert atmosphere
3.1: titanium(IV) isopropylate; diethyl (2S,3S)-tartrate / dichloromethane / 1 h / -25 °C / Inert atmosphere; Molecular sieve
3.2: 17 h / -20 °C / Inert atmosphere; Molecular sieve
4.1: sulfur trioxide pyridine complex; dimethyl sulfoxide; triethylamine / dichloromethane / 0 - 25 °C / Inert atmosphere
5.1: dichloromethane / 14 h / 20 °C / Inert atmosphere
6.1: tetrabutyl ammonium fluoride / dichloromethane / 0.33 h / 0 °C / Inert atmosphere
7.1: pyridinium p-toluenesulfonate / dichloromethane / 25 - 40 °C / Inert atmosphere
8.1: lanthanum(lll) triflate / toluene / 6 h / 25 °C / Inert atmosphere
9.1: sodium tetrahydroborate; nickel (II) chloride hexahydrate / ethanol / 0 °C / Inert atmosphere
10.1: lithium aluminium tetrahydride / tetrahydrofuran; diethyl ether / 0.5 h / 25 °C / Inert atmosphere
11.1: sulfur trioxide pyridine complex; dimethyl sulfoxide; triethylamine / dichloromethane / 0 - 25 °C / Inert atmosphere
12.1: sodium hexamethyldisilazane / tetrahydrofuran; toluene / 0.17 h / 0 °C / Inert atmosphere
12.2: 0.33 h / 0 °C / Inert atmosphere
13.1: 2,3-dicyano-5,6-dichloro-p-benzoquinone / dichloromethane / 3 h / 0 °C / Inert atmosphere
14.1: dmap; 2-methyl-6-nitrobenzoic anhydride; triethylamine / toluene / 0.33 h / 25 °C / Inert atmosphere; Molecular sieve
14.2: 13 h / 25 °C / Inert atmosphere; Molecular sieve
15.1: p-toluenesulfonic acid monohydrate / methanol; dichloromethane / 0.67 h / 0 °C / Inert atmosphere
16.1: N,N,N,N,-tetramethylethylenediamine; titanium tetrachloride / tetrahydrofuran; dichloromethane / 0 - 25 °C / Inert atmosphere
16.2: 0.67 h / 25 °C / Inert atmosphere
With 2,6-dimethylpyridine; titanium(IV) isopropylate; dmap; sodium tetrahydroborate; lithium aluminium tetrahydride; nickel (II) chloride hexahydrate; diethyl (2S,3S)-tartrate; N,N,N,N,-tetramethylethylenediamine; 2-methyl-6-nitrobenzoic anhydride; p-toluenesulfonic acid monohydrate; tetrabutyl ammonium fluoride; sodium hexamethyldisilazane; sulfur trioxide pyridine complex; pyridinium p-toluenesulfonate; titanium tetrachloride; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; lanthanum(lll) triflate; In tetrahydrofuran; methanol; diethyl ether; ethanol; dichloromethane; toluene; 3.1: Sharpless epoxidation / 3.2: Sharpless epoxidation / 4.1: Parikh-Doering oxidation / 5.1: Wittig reaction / 11.1: Parikh-Doering oxidation / 12.1: Wittig reaction / 12.2: Wittig reaction;
DOI:10.1021/ja109533y
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