Technology Process of 7-allyl-6-tosyl-6-azaspiro[4.5]decane
There total 9 articles about 7-allyl-6-tosyl-6-azaspiro[4.5]decane which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
diisobutylaluminium hydride;
In
hexanes; dichloromethane;
at 0 - 20 ℃;
for 2.75h;
Inert atmosphere;
DOI:10.1016/j.tet.2011.04.047
- Guidance literature:
-
Multi-step reaction with 6 steps
1: triethylamine / dichloromethane / 0 - 20 °C / Inert atmosphere
2: 3-chloro-benzenecarboperoxoic acid / chloroform / 10 - 20 °C / Inert atmosphere
3: boron trifluoride diethyl etherate / dichloromethane / 0.75 h / -78 °C / Inert atmosphere
4: (triphenylphosphine)copper(I) hydride hexamer / water; benzene / 20 °C / Inert atmosphere
5: ethanol / 20 °C / Inert atmosphere
6: diisobutylaluminium hydride / hexanes; dichloromethane / 2.75 h / 0 - 20 °C / Inert atmosphere
With
(triphenylphosphine)copper(I) hydride hexamer; boron trifluoride diethyl etherate; diisobutylaluminium hydride; triethylamine; 3-chloro-benzenecarboperoxoic acid;
In
hexanes; ethanol; dichloromethane; chloroform; water; benzene;
2: aza-Achmatowicz rearrangement;
DOI:10.1016/j.tet.2011.04.047
- Guidance literature:
-
Multi-step reaction with 7 steps
1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 1 h
2: triethylamine / dichloromethane / 0 - 20 °C / Inert atmosphere
3: 3-chloro-benzenecarboperoxoic acid / chloroform / 10 - 20 °C / Inert atmosphere
4: boron trifluoride diethyl etherate / dichloromethane / 0.75 h / -78 °C / Inert atmosphere
5: (triphenylphosphine)copper(I) hydride hexamer / water; benzene / 20 °C / Inert atmosphere
6: ethanol / 20 °C / Inert atmosphere
7: diisobutylaluminium hydride / hexanes; dichloromethane / 2.75 h / 0 - 20 °C / Inert atmosphere
With
(triphenylphosphine)copper(I) hydride hexamer; palladium 10% on activated carbon; boron trifluoride diethyl etherate; hydrogen; diisobutylaluminium hydride; triethylamine; 3-chloro-benzenecarboperoxoic acid;
In
hexanes; ethanol; dichloromethane; chloroform; water; ethyl acetate; benzene;
3: aza-Achmatowicz rearrangement;
DOI:10.1016/j.tet.2011.04.047