Technology Process of 3-Hexanol, 2,4,5-trifluoro-1,6-bis(phenylmethoxy)-, (2R,3R,4R,5R)-
There total 5 articles about 3-Hexanol, 2,4,5-trifluoro-1,6-bis(phenylmethoxy)-, (2R,3R,4R,5R)- 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:
-
4,5-bis-(2-benzyloxy-1-fluoroethyl)-[1,3,2]dioxathiolane 2,2-dioxide;
With
tetrabutyl ammonium fluoride;
In
tetrahydrofuran; acetonitrile;
at 0 - 20 ℃;
for 4h;
With
sulfuric acid;
In
tetrahydrofuran;
at 20 ℃;
for 48h;
DOI:10.1021/ja066188p
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: 0.491 g / NaIO4 / RuCl3*H2O / acetonitrile; H2O / 3 h / 0 °C
2.1: tetrabutylammonium fluoride / acetonitrile; tetrahydrofuran / 4 h / 0 - 20 °C
2.2: 62 percent / aq. H2SO4 / tetrahydrofuran / 48 h / 20 °C
With
sodium periodate; tetrabutyl ammonium fluoride;
ruthenium trichloride;
In
tetrahydrofuran; water; acetonitrile;
DOI:10.1021/ja066188p
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: Grubss second generation catalyst / CH2Cl2 / 6 h / Heating
2.1: 60 percent / aq. KMnO4; MgSO4 / ethanol; CH2Cl2 / 20 h / -10 °C
3.1: SOCl2; pyridine / CH2Cl2 / 2 h / 0 °C
4.1: 0.491 g / NaIO4 / RuCl3*H2O / acetonitrile; H2O / 3 h / 0 °C
5.1: tetrabutylammonium fluoride / acetonitrile; tetrahydrofuran / 4 h / 0 - 20 °C
5.2: 62 percent / aq. H2SO4 / tetrahydrofuran / 48 h / 20 °C
With
pyridine; potassium permanganate; sodium periodate; thionyl chloride; tetrabutyl ammonium fluoride; magnesium sulfate;
tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; ruthenium trichloride;
In
tetrahydrofuran; ethanol; dichloromethane; water; acetonitrile;
DOI:10.1021/ja066188p