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tert-butyl [(3R,4Z)-5-ethyl-3-methyl-4,6-heptadienyl]oxydiphenylsilane

Base Information
  • Chemical Name:tert-butyl [(3R,4Z)-5-ethyl-3-methyl-4,6-heptadienyl]oxydiphenylsilane
  • CAS No.:1322669-20-4
  • Molecular Formula:C26H36OSi
  • Molecular Weight:392.657
  • Hs Code.:
tert-butyl [(3R,4Z)-5-ethyl-3-methyl-4,6-heptadienyl]oxydiphenylsilane

Synonyms:tert-butyl [(3R,4Z)-5-ethyl-3-methyl-4,6-heptadienyl]oxydiphenylsilane

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Chemical Property of tert-butyl [(3R,4Z)-5-ethyl-3-methyl-4,6-heptadienyl]oxydiphenylsilane
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Technology Process of tert-butyl [(3R,4Z)-5-ethyl-3-methyl-4,6-heptadienyl]oxydiphenylsilane

There total 8 articles about tert-butyl [(3R,4Z)-5-ethyl-3-methyl-4,6-heptadienyl]oxydiphenylsilane 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:
Multi-step reaction with 8 steps
1: dimethylsulfide borane complex; dihydrogen peroxide; sodium hydroxide / tetrahydrofuran / 4 h / 0 °C
2: 1H-imidazole / dichloromethane / 2 h / 0 - 20 °C
3: water; 2,3-dicyano-5,6-dichloro-p-benzoquinone / dichloromethane / 2.5 h / 0 - 20 °C
4: dimethyl sulfoxide; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / dichloromethane / 2 h / 0 - 20 °C
5: sodium hydride / tetrahydrofuran / 1.5 h / -78 - 0 °C
6: diisobutylaluminium hydride / dichloromethane / 2 h / -78 °C
7: dimethyl sulfoxide; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / dichloromethane / 2 h / 0 - 20 °C
8: n-butyllithium / tetrahydrofuran / 5 h / -78 - 0 °C
With 1H-imidazole; n-butyllithium; dimethylsulfide borane complex; water; dihydrogen peroxide; sodium hydride; diisobutylaluminium hydride; dimethyl sulfoxide; 2,3-dicyano-5,6-dichloro-p-benzoquinone; sodium hydroxide; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In tetrahydrofuran; dichloromethane; 5: Horner-Wadsworth-Emmons olefination;
DOI:10.1016/j.tetlet.2011.05.151
Guidance literature:
Multi-step reaction with 7 steps
1: 1H-imidazole / dichloromethane / 2 h / 0 - 20 °C
2: water; 2,3-dicyano-5,6-dichloro-p-benzoquinone / dichloromethane / 2.5 h / 0 - 20 °C
3: dimethyl sulfoxide; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / dichloromethane / 2 h / 0 - 20 °C
4: sodium hydride / tetrahydrofuran / 1.5 h / -78 - 0 °C
5: diisobutylaluminium hydride / dichloromethane / 2 h / -78 °C
6: dimethyl sulfoxide; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / dichloromethane / 2 h / 0 - 20 °C
7: n-butyllithium / tetrahydrofuran / 5 h / -78 - 0 °C
With 1H-imidazole; n-butyllithium; water; sodium hydride; diisobutylaluminium hydride; dimethyl sulfoxide; 2,3-dicyano-5,6-dichloro-p-benzoquinone; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In tetrahydrofuran; dichloromethane; 4: Horner-Wadsworth-Emmons olefination;
DOI:10.1016/j.tetlet.2011.05.151
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