Technology Process of Cyclohexane, 1-methylene-2-[(methylthio)methyl]-
There total 5 articles about Cyclohexane, 1-methylene-2-[(methylthio)methyl]- 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
potassium tert-butylate;
In
tetrahydrofuran; dichloromethane; tert-butyl alcohol;
at -40 - 20 ℃;
for 10h;
Schlenk technique;
DOI:10.1021/ol5031348
- Guidance literature:
-
Multi-step reaction with 2 steps
1: 2-chloropyridine / dichloromethane / 5 h / -80 - 20 °C / Schlenk technique
2: potassium tert-butylate / tetrahydrofuran; dichloromethane; tert-butyl alcohol / 10 h / -40 - 20 °C / Schlenk technique
With
2-chloropyridine; potassium tert-butylate;
In
tetrahydrofuran; dichloromethane; tert-butyl alcohol;
DOI:10.1021/ol5031348
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: sodium hydride / dimethyl sulfoxide / 0.17 h / 20 °C / Inert atmosphere; Cooling with ice
1.2: 0.5 h / 20 °C / Inert atmosphere
2.1: 2-chloropyridine / dichloromethane / 5 h / -80 - 20 °C / Schlenk technique
3.1: potassium tert-butylate / tetrahydrofuran; dichloromethane; tert-butyl alcohol / 10 h / -40 - 20 °C / Schlenk technique
With
2-chloropyridine; potassium tert-butylate; sodium hydride;
In
tetrahydrofuran; dichloromethane; dimethyl sulfoxide; tert-butyl alcohol;
DOI:10.1021/ol5031348