Technology Process of C16H22BrNO3S
There total 3 articles about C16H22BrNO3S which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
(2-allyl-1-benzenesulfonyl-3-bromo-piperidin-3-yl)-acetic acid ethyl ester;
With
diisobutylaluminium hydride;
In
tetrahydrofuran;
at 20 ℃;
for 5h;
Inert atmosphere;
Cooling with ice;
With
ammonium chloride;
In
tetrahydrofuran; water;
Inert atmosphere;
Saturated solution;
Cooling with ice;
DOI:10.1016/j.tet.2011.08.025
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: N-Bromosuccinimide; boron trifluoride diethyl etherate / dichloromethane / 5.08 h / 20 °C / Inert atmosphere; Cooling with ice
2.1: diisobutylaluminium hydride / tetrahydrofuran / 5 h / 20 °C / Inert atmosphere; Cooling with ice
2.2: Inert atmosphere; Saturated solution; Cooling with ice
With
N-Bromosuccinimide; boron trifluoride diethyl etherate; diisobutylaluminium hydride;
In
tetrahydrofuran; dichloromethane;
DOI:10.1016/j.tet.2011.08.025
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 2 h / Inert atmosphere; Reflux
2.1: N-Bromosuccinimide; boron trifluoride diethyl etherate / dichloromethane / 5.08 h / 20 °C / Inert atmosphere; Cooling with ice
3.1: diisobutylaluminium hydride / tetrahydrofuran / 5 h / 20 °C / Inert atmosphere; Cooling with ice
3.2: Inert atmosphere; Saturated solution; Cooling with ice
With
N-Bromosuccinimide; boron trifluoride diethyl etherate; diisobutylaluminium hydride; 1,8-diazabicyclo[5.4.0]undec-7-ene;
In
tetrahydrofuran; dichloromethane;
DOI:10.1016/j.tet.2011.08.025