Technology Process of (3aS,8aR)-3a-allyl-1,8-dimethyl-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indol-5-yl phenylcarbamate
There total 11 articles about (3aS,8aR)-3a-allyl-1,8-dimethyl-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indol-5-yl phenylcarbamate which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
C15H20N2O;
With
sodium;
In
diethyl ether;
at 20 ℃;
for 0.25h;
Inert atmosphere;
phenyl isocyanate;
In
diethyl ether;
for 0.5h;
Inert atmosphere;
DOI:10.1016/j.bmc.2012.06.048
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: lithium aluminium tetrahydride / tetrahydrofuran / 2.5 h / Inert atmosphere; Reflux
2.1: boron tribromide / dichloromethane / 1.5 h / 0 - 20 °C / Inert atmosphere
2.2: 0.5 h
3.1: sodium / diethyl ether / 0.25 h / 20 °C / Inert atmosphere
3.2: 0.5 h / Inert atmosphere
With
lithium aluminium tetrahydride; sodium; boron tribromide;
In
tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1016/j.bmc.2012.06.048
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: sodium hydride / tetrahydrofuran / 2 h / 0 °C / Inert atmosphere
1.2: 0.5 h / Inert atmosphere
2.1: lithium hydroxide monohydrate; dihydrogen peroxide / tetrahydrofuran; water / 72 h / 20 °C
3.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / tetrahydrofuran / 2 h / 20 °C / Inert atmosphere
4.1: tetrahydrofuran
5.1: lithium aluminium tetrahydride / tetrahydrofuran / 2.5 h / Inert atmosphere; Reflux
6.1: boron tribromide / dichloromethane / 1.5 h / 0 - 20 °C / Inert atmosphere
6.2: 0.5 h
7.1: sodium / diethyl ether / 0.25 h / 20 °C / Inert atmosphere
7.2: 0.5 h / Inert atmosphere
With
lithium aluminium tetrahydride; lithium hydroxide monohydrate; dihydrogen peroxide; sodium; boron tribromide; sodium hydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine;
In
tetrahydrofuran; diethyl ether; dichloromethane; water;
DOI:10.1016/j.bmc.2012.06.048