Technology Process of C13H18O2
There total 5 articles about C13H18O2 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
C23H32N2O2Si; lithium perchlorate;
In
diethyl ether; dichloromethane;
at -40 ℃;
for 19h;
enantioselective reaction;
Inert atmosphere;
DOI:10.1002/anie.201202643
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / toluene / 2 h / 40 °C / Inert atmosphere
2.1: lithium borohydride / tetrahydrofuran; methanol / 2 h / 0 °C / Inert atmosphere
3.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 0.25 h / -78 °C / Inert atmosphere
3.2: 1.5 h / -78 - 0 °C / Inert atmosphere
4.1: C23H32N2O2Si; lithium perchlorate / diethyl ether; dichloromethane / 19 h / -40 °C / Inert atmosphere
With
tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; lithium borohydride; oxalyl dichloride; C23H32N2O2Si; lithium perchlorate; dimethyl sulfoxide;
In
tetrahydrofuran; methanol; diethyl ether; dichloromethane; toluene;
3.1: Swern oxidation / 3.2: Swern oxidation;
DOI:10.1002/anie.201202643
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: sodium hexamethyldisilazane / tetrahydrofuran / -78 °C / Inert atmosphere
1.2: -40 °C / Inert atmosphere
2.1: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / toluene / 2 h / 40 °C / Inert atmosphere
3.1: lithium borohydride / tetrahydrofuran; methanol / 2 h / 0 °C / Inert atmosphere
4.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 0.25 h / -78 °C / Inert atmosphere
4.2: 1.5 h / -78 - 0 °C / Inert atmosphere
5.1: C23H32N2O2Si; lithium perchlorate / diethyl ether; dichloromethane / 19 h / -40 °C / Inert atmosphere
With
tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; lithium borohydride; oxalyl dichloride; C23H32N2O2Si; lithium perchlorate; sodium hexamethyldisilazane; dimethyl sulfoxide;
In
tetrahydrofuran; methanol; diethyl ether; dichloromethane; toluene;
4.1: Swern oxidation / 4.2: Swern oxidation;
DOI:10.1002/anie.201202643