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C49H64N2O11Si

Base Information
  • Chemical Name:C49H64N2O11Si
  • CAS No.:1404078-85-8
  • Molecular Formula:C49H64N2O11Si
  • Molecular Weight:885.139
  • Hs Code.:
C<sub>49</sub>H<sub>64</sub>N<sub>2</sub>O<sub>11</sub>Si

Synonyms:C49H64N2O11Si

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Chemical Property of C49H64N2O11Si
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Technology Process of C49H64N2O11Si

There total 15 articles about C49H64N2O11Si 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 triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; toluene; at 0 - 20 ℃; for 0.5h;
DOI:10.1039/c2ob26256h
Guidance literature:
Multi-step reaction with 11 steps
1.1: titanium tetrachloride / dichloromethane / 0.33 h / -50 °C
1.2: 2 h / -40 °C
1.3: 2 h / -78 °C
2.1: 2,6-dimethylpyridine / dichloromethane / 3 h / -78 - 20 °C
3.1: dihydrogen peroxide; lithium hydroxide / tetrahydrofuran; water / 3 h / 0 - 20 °C
4.1: N-ethyl-N,N-diisopropylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; benzotriazol-1-ol / dichloromethane / 2 h / 20 °C
4.2: 72 h / 20 °C
5.1: diethylamino-sulfur trifluoride / dichloromethane / 2 h / -78 °C
6.1: copper(ll) bromide; hexamethylenetetramine; 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 2 h / 20 °C
7.1: diisobutylaluminium hydride / dichloromethane; toluene / 0.75 h / -78 °C
8.1: potassium carbonate / methanol / 0 - 20 °C
9.1: Schwartz's reagent / tetrahydrofuran / 1 h / 0 °C
9.2: 0.67 h / -78 °C / Darkness
10.1: tert.-butyl lithium / pentane; diethyl ether / 1 h / -78 °C / Inert atmosphere
10.2: 0.25 h / -78 °C
10.3: 3 h / -78 °C
11.1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran; toluene / 0.5 h / 0 - 20 °C
With 2,6-dimethylpyridine; Schwartz's reagent; diethylamino-sulfur trifluoride; hexamethylenetetramine; dihydrogen peroxide; tert.-butyl lithium; titanium tetrachloride; diisobutylaluminium hydride; potassium carbonate; benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; 1,8-diazabicyclo[5.4.0]undec-7-ene; N-ethyl-N,N-diisopropylamine; triphenylphosphine; copper(ll) bromide; lithium hydroxide; diethylazodicarboxylate; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; water; toluene; pentane;
DOI:10.1039/c2ob26256h
Guidance literature:
Multi-step reaction with 10 steps
1.1: 2,6-dimethylpyridine / dichloromethane / 3 h / -78 - 20 °C
2.1: dihydrogen peroxide; lithium hydroxide / tetrahydrofuran; water / 3 h / 0 - 20 °C
3.1: N-ethyl-N,N-diisopropylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; benzotriazol-1-ol / dichloromethane / 2 h / 20 °C
3.2: 72 h / 20 °C
4.1: diethylamino-sulfur trifluoride / dichloromethane / 2 h / -78 °C
5.1: copper(ll) bromide; hexamethylenetetramine; 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 2 h / 20 °C
6.1: diisobutylaluminium hydride / dichloromethane; toluene / 0.75 h / -78 °C
7.1: potassium carbonate / methanol / 0 - 20 °C
8.1: Schwartz's reagent / tetrahydrofuran / 1 h / 0 °C
8.2: 0.67 h / -78 °C / Darkness
9.1: tert.-butyl lithium / pentane; diethyl ether / 1 h / -78 °C / Inert atmosphere
9.2: 0.25 h / -78 °C
9.3: 3 h / -78 °C
10.1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran; toluene / 0.5 h / 0 - 20 °C
With 2,6-dimethylpyridine; Schwartz's reagent; diethylamino-sulfur trifluoride; hexamethylenetetramine; dihydrogen peroxide; tert.-butyl lithium; diisobutylaluminium hydride; potassium carbonate; benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; 1,8-diazabicyclo[5.4.0]undec-7-ene; N-ethyl-N,N-diisopropylamine; triphenylphosphine; copper(ll) bromide; lithium hydroxide; diethylazodicarboxylate; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; water; toluene; pentane;
DOI:10.1039/c2ob26256h
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