Technology Process of Methanone, (2-chlorotetrahydro-1,1-dioxido-2H-thiopyran-2-yl)phenyl-
There total 4 articles about Methanone, (2-chlorotetrahydro-1,1-dioxido-2H-thiopyran-2-yl)phenyl- which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
N-chloro-succinimide; sodium hydride;
In
tetrahydrofuran;
1.) rt, 30 min, 2.) reflux, 90 min;
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 79 percent / NaH, n-BuLi / tetrahydrofuran; hexane; petroleum ether / 1.) THF, petroleum ether, 0 deg C, 30 min, 2.) hexane, 3.) THF, 0 deg C, 3h, 4.) up to rt
2: 93 percent / NaI / acetone / 3 h / Heating
3: 90 percent / aq. NaOH / ethylhexadecyldimethyl ammonium bromide / CH2Cl2 / 1 h
4: 73 percent / NaH, N-chlorosuccinimide / tetrahydrofuran / 1.) rt, 30 min, 2.) reflux, 90 min
With
sodium hydroxide; N-chloro-succinimide; n-butyllithium; sodium hydride; sodium iodide;
hexadecyldimethylethylammonium bromide;
In
tetrahydrofuran; hexane; dichloromethane; acetone; Petroleum ether;
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 93 percent / NaI / acetone / 3 h / Heating
2: 90 percent / aq. NaOH / ethylhexadecyldimethyl ammonium bromide / CH2Cl2 / 1 h
3: 73 percent / NaH, N-chlorosuccinimide / tetrahydrofuran / 1.) rt, 30 min, 2.) reflux, 90 min
With
sodium hydroxide; N-chloro-succinimide; sodium hydride; sodium iodide;
hexadecyldimethylethylammonium bromide;
In
tetrahydrofuran; dichloromethane; acetone;