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C44H75IOSi

Base Information Edit
C<sub>44</sub>H<sub>75</sub>IOSi

Synonyms:C44H75IOSi

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Chemical Property of C44H75IOSi Edit
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Technology Process of C44H75IOSi

There total 27 articles about C44H75IOSi 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 1H-imidazole; iodine; triphenylphosphine; In diethyl ether; acetonitrile; at 20 ℃; for 0.25h; Inert atmosphere;
DOI:10.1002/anie.201303776
Guidance literature:
C35H61NO5; With 1H-imidazole; dmap; tert-butyldimethylsilyl chloride; In dichloromethane; at 20 ℃; for 0.5h; Inert atmosphere;
With potassium carbonate; In methanol; for 6h; Reflux; Inert atmosphere;
tert-butyldiphenylsilyl triflate; Further stages;
DOI:10.1002/chem.201404034
Guidance literature:
Multi-step reaction with 12 steps
1.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 2 h / 0 °C / Inert atmosphere
2.1: water; sodium hydroxide / methanol / 1 h / Reflux
3.1: methyllithium / tetrahydrofuran / 0.67 h / -20 - 20 °C / Inert atmosphere
3.2: 1 h / 40 °C / Inert atmosphere
3.3: 0.25 h / 0 °C / Inert atmosphere
4.1: tert.-butyl lithium / diethyl ether; pentane / 0.17 h / -78 °C / Inert atmosphere
4.2: 2 h / -78 - 20 °C / Inert atmosphere
4.3: 2 h / 20 °C / Darkness
5.1: pyridine / dichloromethane / 1 h / 0 °C / Inert atmosphere
6.1: tetra-N-butylammonium tribromide / methanol / 4 h / 20 °C / Inert atmosphere
7.1: hydrogen; [Ir(cod)(SIMes)(Pyr)]+PF6- / dichloromethane / 18 h / 20 °C / 67506.8 Torr / Autoclave
8.1: 1H-imidazole; dmap / dichloromethane / 0.5 h / 20 °C / Inert atmosphere
9.1: potassium carbonate / methanol / 6 h / 60 °C / Inert atmosphere
10.1: 2,6-dimethylpyridine / dichloromethane / 5 h / 0 °C / Inert atmosphere
11.1: tetra-N-butylammonium tribromide / methanol; tetrahydrofuran / 3 h / 20 °C / Inert atmosphere
12.1: triphenylphosphine; iodine; 1H-imidazole / acetonitrile; diethyl ether / 0.25 h / 20 °C / Inert atmosphere
With pyridine; 1H-imidazole; 2,6-dimethylpyridine; dmap; di-isopropyl azodicarboxylate; [Ir(cod)(SIMes)(Pyr)]+PF6-; water; methyllithium; hydrogen; iodine; tert.-butyl lithium; tetra-N-butylammonium tribromide; potassium carbonate; triphenylphosphine; sodium hydroxide; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; acetonitrile; pentane;
DOI:10.1002/anie.201303776
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