Technology Process of methyl thiomethylpluviatilol
There total 7 articles about methyl thiomethylpluviatilol 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:
-
With
triethylsilane; boron trifluoride diethyl etherate;
In
dichloromethane;
for 48h;
Ambient temperature;
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 1) di-isopropylamine, n-butyl-lithium / tetrahydrofuran / 1.) -10 to -78 deg C, 1 h, 2.) -78 deg C, 45 min
2: 81 percent / DIBAL / tetrahydrofuran / 3 h / -78 - -40 °C
3: 67 percent / cc HCl / 0.5 h / Heating
4: 88.5 percent / triethylsilane, BF3-ether / CH2Cl2 / 48 h / Ambient temperature
With
hydrogenchloride; triethylsilane; n-butyllithium; boron trifluoride diethyl etherate; diisobutylaluminium hydride; diisopropylamine;
In
tetrahydrofuran; dichloromethane;
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 1) di-isopropylamine, n-butyl-lithium / tetrahydrofuran / 1.) -10 to -78 deg C, 1 h, 2.) -78 deg C, 45 min
2: 81 percent / DIBAL / tetrahydrofuran / 3 h / -78 - -40 °C
3: 67 percent / cc HCl / 0.5 h / Heating
4: 88.5 percent / triethylsilane, BF3-ether / CH2Cl2 / 48 h / Ambient temperature
With
hydrogenchloride; triethylsilane; n-butyllithium; boron trifluoride diethyl etherate; diisobutylaluminium hydride; diisopropylamine;
In
tetrahydrofuran; dichloromethane;
