Technology Process of 2-(4-METHOXY-PHENYL)-MORPHOLINE HYDROCHLORIDE
There total 7 articles about 2-(4-METHOXY-PHENYL)-MORPHOLINE HYDROCHLORIDE 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:
-
C18H21NO2;
With
carbonochloridic acid 1-chloro-ethyl ester;
In
dichloromethane;
at 20 ℃;
With
methanol;
Reflux;
DOI:10.1016/j.bmcl.2013.09.020
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: lithium borohydride; chloro-trimethyl-silane / tetrahydrofuran / 20 °C
2.1: carbonochloridic acid 1-chloro-ethyl ester / dichloromethane / 20 °C
2.2: Reflux
With
lithium borohydride; chloro-trimethyl-silane; carbonochloridic acid 1-chloro-ethyl ester;
In
tetrahydrofuran; dichloromethane;
DOI:10.1016/j.bmcl.2013.09.020
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: borane-THF; potassium hydroxide; (S)-Corey-Bakshi-Shibata oxazaborolidine / water; diethyl ether / -30 °C
2.1: potassium hydroxide / water; diethyl ether / 20 °C
3.1: 80 °C
4.1: sodium hydroxide / dichloromethane; water / 20 °C
5.1: potassium hydroxide / isopropyl alcohol / 20 °C
6.1: lithium borohydride; chloro-trimethyl-silane / tetrahydrofuran / 20 °C
7.1: carbonochloridic acid 1-chloro-ethyl ester / dichloromethane / 20 °C
7.2: Reflux
With
lithium borohydride; chloro-trimethyl-silane; borane-THF; carbonochloridic acid 1-chloro-ethyl ester; potassium hydroxide; sodium hydroxide; (S)-Corey-Bakshi-Shibata oxazaborolidine;
In
tetrahydrofuran; diethyl ether; dichloromethane; water; isopropyl alcohol;
DOI:10.1016/j.bmcl.2013.09.020