Technology Process of 1-(2-(bromomethyl)-3-chlorophenyl)cyclobutanol
There total 5 articles about 1-(2-(bromomethyl)-3-chlorophenyl)cyclobutanol which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: lithium diisopropyl amide / tetrahydrofuran / 1 h / -70 °C
1.2: 1 h
2.1: potassium borohydride / ethanol / 2 h / 0 °C
3.1: toluene-4-sulfonic acid / tetrahydrofuran / 4 h / 5 °C
4.1: n-butyllithium / tetrahydrofuran / 0.5 h / -70 °C
4.2: 1 h / -70 °C
5.1: toluene-4-sulfonic acid / dichloromethane; methanol / 2 h / 5 °C
6.1: N-Bromosuccinimide; triphenylphosphine / dichloromethane / 2 h / 5 °C
With
N-Bromosuccinimide; n-butyllithium; potassium borohydride; toluene-4-sulfonic acid; triphenylphosphine; lithium diisopropyl amide;
In
tetrahydrofuran; methanol; ethanol; dichloromethane;
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: potassium borohydride / ethanol / 2 h / 0 °C
2.1: toluene-4-sulfonic acid / tetrahydrofuran / 4 h / 5 °C
3.1: n-butyllithium / tetrahydrofuran / 0.5 h / -70 °C
3.2: 1 h / -70 °C
4.1: toluene-4-sulfonic acid / dichloromethane; methanol / 2 h / 5 °C
5.1: N-Bromosuccinimide; triphenylphosphine / dichloromethane / 2 h / 5 °C
With
N-Bromosuccinimide; n-butyllithium; potassium borohydride; toluene-4-sulfonic acid; triphenylphosphine;
In
tetrahydrofuran; methanol; ethanol; dichloromethane;
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: n-butyllithium / tetrahydrofuran / 0.5 h / -70 °C
1.2: 1 h / -70 °C
2.1: toluene-4-sulfonic acid / dichloromethane; methanol / 2 h / 5 °C
3.1: N-Bromosuccinimide; triphenylphosphine / dichloromethane / 2 h / 5 °C
With
N-Bromosuccinimide; n-butyllithium; toluene-4-sulfonic acid; triphenylphosphine;
In
tetrahydrofuran; methanol; dichloromethane;