Double-tail gemini quaternary ammonium salt type cationic surface active agent and preparation method thereof
A technology of gemini quaternary ammonium salt and surfactant is applied in the field of long-chain aliphatic amine derivatives and their preparation, which can solve the problem of not finding research reports on double-tailed gemini cationic surfactants, and achieve good lipophilic performance and reaction Mild conditions and highly ordered effects
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Embodiment 1
[0029] Accurately weigh 15.414g (0.042mol) of behenylmethyl tertiary amine in a two-necked flask equipped with a reflux condenser, add 4.04g (0.02mol) of dibromo-n-propane at room temperature, add 20ml of acetonitrile, and After injecting nitrogen gas for 20 minutes, the reaction was performed under magnetic stirring at 83° C. for 10 to 15 hours. After the reaction, the solvent was distilled off under reduced pressure to obtain a yellowish colloidal substance, which was precipitated at low temperature by adding acetone, filtered, washed twice with acetone, and dried in vacuo to obtain a white powdery solid 212-3-212.
Embodiment 2
[0031] Accurately weigh 15.414g (0.042mol) of behenylmethyl tertiary amine in a two-necked flask equipped with a reflux condenser, add 4.32g (0.02mol) of dibromobutane at room temperature, add 20ml of acetonitrile, After passing nitrogen gas for 20 minutes, the reaction was performed under magnetic stirring at 83° C. for 10 to 15 hours. After the reaction, the solvent was distilled off under reduced pressure to obtain a yellowish colloidal substance, which was precipitated at low temperature by adding acetone, filtered and washed twice with acetone, and dried in vacuum to obtain a white powdery solid 212-4-212.
Embodiment 3
[0033] Accurately weigh 15.414g (0.042mol) of behenylmethyl tertiary amine in a two-necked flask equipped with a reflux condenser, add 4.88g (0.02mol) of dibromo-n-hexane at room temperature, add 20ml of acetonitrile, and After injecting nitrogen gas for 20 minutes, the reaction was performed under magnetic stirring at 83° C. for 10 to 15 hours. After the reaction, the solvent was distilled off under reduced pressure to obtain a yellowish colloidal substance, which was precipitated at low temperature by adding acetone, filtered and washed twice with acetone, and dried in vacuum to obtain a white powdery solid 212-6-212.
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