Method for preparing 4-vinyl benzyl surface-active macromonomer
A vinylbenzyl-type, surface-active technology, which is applied in chemical instruments and methods, drilling compositions, transportation and packaging, etc., can solve the problem of low surface activity, achieve enhanced oil recovery, and increase rigidity , Improve the effect of temperature resistance and thermal stability
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Embodiment 1
[0020] Add 20 parts of octylphenol polyoxyethylene ether (the adduct EO of polyoxyethylene ether is 10), 18 parts of solvent acetone, and 0.5 parts of catalyst sodium into a three-necked reaction flask equipped with a reflux condensation device, and stir the reaction at room temperature After 1h, the temperature was raised to 45°C, 3 parts of 4 vinylbenzyl chloride were added, and the reaction was continued for 6 hours. The solvent was distilled off from the reaction product under reduced pressure to obtain a crude product, which was then separated by silica gel column chromatography to obtain 4-vinylbenzylalkylphenol polyoxyethylene ether with a yield of 61%.
Embodiment 2
[0022] Add 20 parts of nonylphenol polyoxyethylene ether (the adduct EO of polyoxyethylene ether is 20), 60 parts of solvent N, N-dimethylformamide, and 2.3 parts of catalyst sodium hydride into the three-port port equipped with a reflux condensing device. In the reaction flask, the reaction was stirred at room temperature for 1 h, then the temperature was raised to 60° C., 5.5 parts of 4-vinylbenzyl chloride was added, and the reaction was continued for 24 hours. The solvent was distilled off from the reaction product under reduced pressure to obtain a crude product, which was then separated by silica gel column chromatography to obtain 4-vinylbenzylalkylphenol polyoxyethylene ether with a yield of 74%.
Embodiment 3
[0024] Add 20 parts of dodecylphenol polyoxyethylene ether (the adduct EO of polyoxyethylene ether is 15), 150 parts of solvent tetrahydrofuran, and 5.8 parts of catalyst sodium carbonate into a three-necked reaction flask equipped with a reflux condensation device. The reaction was stirred for 1 h, then the temperature was raised to 60° C., 22 parts of 4-vinylbenzyl chloride were added, and the reaction was continued for 24 hours. The solvent was distilled off from the reaction product under reduced pressure to obtain a crude product, which was then separated by silica gel column chromatography to obtain 4-vinylbenzylalkylphenol polyoxyethylene ether with a yield of 92%.
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