Technology Process of (S)-5-(benzyloxy)hept-1-ene
There total 2 articles about (S)-5-(benzyloxy)hept-1-ene 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:
-
(R)-3-(benzyloxy)hept-6-en-1-yl p-toluenesulfonate;
With
lithium triethylborohydride;
In
tetrahydrofuran;
at 0 - 20 ℃;
for 2h;
Inert atmosphere;
With
ammonium chloride;
In
tetrahydrofuran; water;
DOI:10.1016/j.tetasy.2012.06.009
- Guidance literature:
-
Multi-step reaction with 3 steps
1: tetrabutyl ammonium fluoride / tetrahydrofuran / 62 h / 20 °C / Inert atmosphere
2: pyridine / 15 h / 0 °C / Inert atmosphere
3: lithium triethylborohydride / tetrahydrofuran / 2 h / 0 - 20 °C / Inert atmosphere
With
pyridine; tetrabutyl ammonium fluoride; lithium triethylborohydride;
In
tetrahydrofuran;
DOI:10.1016/j.tetasy.2012.06.009
- Guidance literature:
-
Multi-step reaction with 2 steps
1: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / dichloromethane / 2 h / 45 °C / Inert atmosphere
2: lithium tetrafluoroborate / water; acetonitrile / 1 h / 20 °C / Inert atmosphere
With
tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; lithium tetrafluoroborate;
In
dichloromethane; water; acetonitrile;
DOI:10.1016/j.tetasy.2012.06.009