A kind of four-quaternary phosphonium cationic antibacterial agent containing dihydroxy and preparation method thereof
A phosphonium cation and dihydroxyl technology is applied in the field of four-season phosphonium cation antibacterial agent and its preparation, which can solve the problems of limited use range, no research on four-season phosphonium salt, and reduced quaternary phosphonium salt grafting rate, etc., and achieves high-efficiency and broad-spectrum antibacterial properties , long-lasting antibacterial effect
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Embodiment 1
[0036] First synthesize compound B1: Take 1,6-bis(diphenylphosphine)hexane (1.14g, 2.5mmol), p-bromophenol (2.16g, 12.5mmol), 5mL of ethylene glycol and 50mg of nickel bromide into 50mL In a three-neck flask, nitrogen gas was introduced, and the temperature was raised to 180° C. under reflux. After 4 hours of magnetic stirring reaction, the system was left to stand, and after cooling, all the reactants were dissolved in 20 mL of dichloromethane, and the organic layer was washed three times with deionized water. anhydrous Na 2 SO 4 The solution was dried and filtered, and the organic phase was washed with a large amount of diethyl ether and a large amount of tetrahydrofuran, respectively, to obtain compound B1.
[0037] Take compound A1 (0.4g, 1.64mmol), and compound B1 (2.3g, 3.61mmol), potassium carbonate (1.0g, 7.24mmol), DMF 20mL were added to a 100mL single-necked flask, magnetically stirred at reflux at 50°C 8h. Cool to room temperature after the reaction is complete....
Embodiment 2
[0039]Take compound A2 (0.5g, 1.64mmol), add compound B1 (2.3g, 3.61mmol), sodium carbonate (0.7g, 7.24mmol), and DMF 20mL into a 100mL single-necked flask, and magnetically stir and reflux at 50°C 8h. Cool to room temperature after the reaction is complete. All reactants were then dissolved in 20 mL of dichloromethane. The organic layer was washed three times with deionized water, followed by anhydrous Na 2 SO 4 The solution was dried and filtered, and the organic phase was washed with a large amount of tetrahydrofuran to obtain the target compound as a white powder.
Embodiment 3
[0041] Take compound A3 (0.35g, 1.64mmol), add compound B1 (2.3g, 3.61mmol), potassium carbonate (1.0g, 7.24mmol), and dichloromethane 20mL into a 100mL single-necked flask, and magnetically Stir for 24h. Cool to room temperature after the reaction is complete. All reactants were then dissolved in 20 mL of dichloromethane. The organic layer was washed three times with deionized water, followed by anhydrous Na 2 SO 4 The solution was dried and filtered, and the organic phase was washed with a large amount of tetrahydrofuran to obtain the target product in the form of white powder.
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