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C61H85NO12Si

Base Information
  • Chemical Name:C61H85NO12Si
  • CAS No.:1448230-76-9
  • Molecular Formula:C61H85NO12Si
  • Molecular Weight:1052.43
  • Hs Code.:
C<sub>61</sub>H<sub>85</sub>NO<sub>12</sub>Si

Synonyms:C61H85NO12Si

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Chemical Property of C61H85NO12Si
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Technology Process of C61H85NO12Si

There total 15 articles about C61H85NO12Si 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 pyridine; silver nitrate; In N,N-dimethyl-formamide; at 20 ℃; for 1h;
DOI:10.1021/ol4017518
Guidance literature:
Multi-step reaction with 10 steps
1.1: 9-methoxy-9-BBN; tert.-butyl lithium / tetrahydrofuran; hexane; diethyl ether; pentane / 4 h / -78 - 20 °C
1.2: 0.33 h / 20 °C
1.3: 13 h / 50 °C
2.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 3 h / 20 °C
3.1: pyridinium p-toluenesulfonate / dichloromethane / 7.5 h / 0 - 20 °C
4.1: acetic acid / tetrahydrofuran; water / 16 h / 20 °C
5.1: pyridinium p-toluenesulfonate / dichloromethane / 2 h / 20 °C
6.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 - 20 °C
6.2: 12 h / 0 - 20 °C
7.1: diisobutylaluminium hydride / dichloromethane; hexane / 2.25 h / -78 °C
8.1: triethylamine; sulfur trioxide pyridine complex / dichloromethane; dimethyl sulfoxide / 2 h / 0 °C
9.1: triethylamine; di-n-butylboryl trifluoromethanesulfonate / dichloromethane / 1 h / 0 °C
9.2: 2.25 h / -78 - 0 °C
9.3: 1 h / 0 °C
10.1: pyridine; silver nitrate / N,N-dimethyl-formamide / 1 h / 20 °C
With pyridine; di-n-butylboryl trifluoromethanesulfonate; tetrabutyl ammonium fluoride; tert.-butyl lithium; sulfur trioxide pyridine complex; pyridinium p-toluenesulfonate; sodium hydride; diisobutylaluminium hydride; silver nitrate; acetic acid; triethylamine; 9-methoxy-9-BBN; In tetrahydrofuran; diethyl ether; hexane; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; mineral oil; pentane; 9.1: |Evans Aldol Reaction / 9.2: |Evans Aldol Reaction;
DOI:10.1021/ol4017518
Guidance literature:
Multi-step reaction with 14 steps
1.1: 2,6-dimethylpyridine / dichloromethane / 0 - 20 °C
2.1: 2,3-dicyano-5,6-dichloro-p-benzoquinone / dichloromethane / 1.17 h / 20 °C / pH 7
3.1: triethylamine; dmap / dichloromethane / 25 h / 0 - 20 °C
4.1: sodium iodide / acetone / 18 h / 50 °C
5.1: 9-methoxy-9-BBN; tert.-butyl lithium / tetrahydrofuran; hexane; diethyl ether; pentane / 4 h / -78 - 20 °C
5.2: 0.33 h / 20 °C
5.3: 13 h / 50 °C
6.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 3 h / 20 °C
7.1: pyridinium p-toluenesulfonate / dichloromethane / 7.5 h / 0 - 20 °C
8.1: acetic acid / tetrahydrofuran; water / 16 h / 20 °C
9.1: pyridinium p-toluenesulfonate / dichloromethane / 2 h / 20 °C
10.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 - 20 °C
10.2: 12 h / 0 - 20 °C
11.1: diisobutylaluminium hydride / dichloromethane; hexane / 2.25 h / -78 °C
12.1: triethylamine; sulfur trioxide pyridine complex / dichloromethane; dimethyl sulfoxide / 2 h / 0 °C
13.1: triethylamine; di-n-butylboryl trifluoromethanesulfonate / dichloromethane / 1 h / 0 °C
13.2: 2.25 h / -78 - 0 °C
13.3: 1 h / 0 °C
14.1: pyridine; silver nitrate / N,N-dimethyl-formamide / 1 h / 20 °C
With pyridine; 2,6-dimethylpyridine; dmap; di-n-butylboryl trifluoromethanesulfonate; tetrabutyl ammonium fluoride; tert.-butyl lithium; sulfur trioxide pyridine complex; pyridinium p-toluenesulfonate; sodium hydride; diisobutylaluminium hydride; silver nitrate; acetic acid; triethylamine; 9-methoxy-9-BBN; 2,3-dicyano-5,6-dichloro-p-benzoquinone; sodium iodide; In tetrahydrofuran; diethyl ether; hexane; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; acetone; mineral oil; pentane; 13.1: |Evans Aldol Reaction / 13.2: |Evans Aldol Reaction;
DOI:10.1021/ol4017518
upstream raw materials:

C22H36O6

C32H68O5Si2

C39H74O7SSi2

C32H67IO4Si2

Downstream raw materials:

C56H78O14

C54H76O13

C60H90O13Si

C57H86O12Si

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