Technology Process of Benzenemethanol,
2-[[(1E)-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-penten-1-yl]dimethylsil
yl]-
There total 9 articles about Benzenemethanol,
2-[[(1E)-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-penten-1-yl]dimethylsil
yl]- 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 5 steps
1: 83 percent / p-toluenesulfonic acid monohydrate / methanol / 16 h / 20 °C
2: LiAlH4 / diethyl ether / 1.67 h / 20 °C
3: diethyl ether / 0 - 20 °C
4: (t-Bu)3P / Pt(1,3-divinyl-1,1,3,3-tetramethyldisiloxane) / hexane / 3 h / 20 °C
5: K2CO3 / methanol; H2O / 50 °C
With
lithium aluminium tetrahydride; tri-tert-butyl phosphine; potassium carbonate; toluene-4-sulfonic acid;
Pt(1,3-divinyl-1,1,3,3-tetramethyldisiloxane);
In
methanol; diethyl ether; hexane; water;
DOI:10.1016/j.jorganchem.2006.04.046
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: n-BuLi / tetrahydrofuran; hexane / 0.67 h / -78 °C
1.2: 83 percent / tetrahydrofuran; hexane / -78 - 20 °C
2.1: 83 percent / p-toluenesulfonic acid monohydrate / methanol / 16 h / 20 °C
3.1: LiAlH4 / diethyl ether / 1.67 h / 20 °C
4.1: diethyl ether / 0 - 20 °C
5.1: (t-Bu)3P / Pt(1,3-divinyl-1,1,3,3-tetramethyldisiloxane) / hexane / 3 h / 20 °C
6.1: K2CO3 / methanol; H2O / 50 °C
With
lithium aluminium tetrahydride; n-butyllithium; tri-tert-butyl phosphine; potassium carbonate; toluene-4-sulfonic acid;
Pt(1,3-divinyl-1,1,3,3-tetramethyldisiloxane);
In
tetrahydrofuran; methanol; diethyl ether; hexane; water;
DOI:10.1016/j.jorganchem.2006.04.046
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: conc. hydrochloric acid / 20 °C
2.1: n-BuLi / tetrahydrofuran; hexane / 0.67 h / -78 °C
2.2: 83 percent / tetrahydrofuran; hexane / -78 - 20 °C
3.1: 83 percent / p-toluenesulfonic acid monohydrate / methanol / 16 h / 20 °C
4.1: LiAlH4 / diethyl ether / 1.67 h / 20 °C
5.1: diethyl ether / 0 - 20 °C
6.1: (t-Bu)3P / Pt(1,3-divinyl-1,1,3,3-tetramethyldisiloxane) / hexane / 3 h / 20 °C
7.1: K2CO3 / methanol; H2O / 50 °C
With
hydrogenchloride; lithium aluminium tetrahydride; n-butyllithium; tri-tert-butyl phosphine; potassium carbonate; toluene-4-sulfonic acid;
Pt(1,3-divinyl-1,1,3,3-tetramethyldisiloxane);
In
tetrahydrofuran; methanol; diethyl ether; hexane; water;
DOI:10.1016/j.jorganchem.2006.04.046