Technology Process of ethyl 7-(4-fluorobenzylidenimino)-8-methylnonanoate
There total 4 articles about ethyl 7-(4-fluorobenzylidenimino)-8-methylnonanoate which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 85 percent / N-bromosuccinimide / CCl4 / 5 h / Heating
2: 55 percent / lithium bromide / dimethylformamide / 1 h / 95 °C
3: 75 percent / hydroxylammonium chloride / ethanol / 5 h / Heating
4: 1.) zinc powder, acetic acid / 1.) room temperature, 2.) room temperature, 2 h
With
N-Bromosuccinimide; hydroxylamine hydrochloride; acetic acid; lithium bromide; zinc;
In
tetrachloromethane; ethanol; N,N-dimethyl-formamide;
- Guidance literature:
-
Multi-step reaction with 2 steps
1: 75 percent / hydroxylammonium chloride / ethanol / 5 h / Heating
2: 1.) zinc powder, acetic acid / 1.) room temperature, 2.) room temperature, 2 h
With
hydroxylamine hydrochloride; acetic acid; zinc;
In
ethanol;
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 55 percent / lithium bromide / dimethylformamide / 1 h / 95 °C
2: 75 percent / hydroxylammonium chloride / ethanol / 5 h / Heating
3: 1.) zinc powder, acetic acid / 1.) room temperature, 2.) room temperature, 2 h
With
hydroxylamine hydrochloride; acetic acid; lithium bromide; zinc;
In
ethanol; N,N-dimethyl-formamide;