A kind of preparation method of antibacterial veterinary drug quinocetone
A technology of quinocetone and acetone, applied in the field of veterinary medicine, can solve the problems of unstable catalyst sodium n-butoxide, difficult to large-scale industrial production, corrosiveness and toxicity, etc., and achieves the advantages of overcoming unstable catalyst, avoiding pollution and short reaction time. Effect
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Embodiment 1-2
[0019] Preparation of alkaline ionic liquid:
[0020] Reflux of N-methylimidazole with excess chloro-n-butane in toluene for 48 hours affords the chloride salt of 1-butyl-3-methylimidazole. Use this chloride salt to separate with NH 4 OH, NH 4 HCO 3 After carrying out ion exchange reaction in acetonitrile solution, filter, remove solvent, and vacuum dry to obtain corresponding basic ionic liquid 1 and basic ionic liquid 2, respectively, as shown in the following formula:
[0021] , .
Embodiment 3
[0023] Reflux of N-methylpyrrole with excess chloro-n-butane in toluene for 48 hours affords the chloride salt of 1-butyl-1-methylpyrrole. Use this chloride salt with NH 4 HCO 3 After carrying out the ion exchange reaction in the acetonitrile solution, filter, remove the solvent, and vacuum dry to obtain the corresponding basic ionic liquid 3 respectively, as shown in the following formula:
[0024] .
Embodiment 4
[0026] Reflux of N-methylpiperidine with excess chloro-n-butane in toluene for 48 hours gave 1-butyl-1-methylpiperidine as the chloride salt. Use this chloride salt with NH 4 HCO 3 After carrying out ion exchange reaction in acetonitrile solution, filter, remove solvent, and vacuum dry to obtain corresponding basic ionic liquid 4, as shown in the following formula:
[0027] .
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