Long-chain alkyl quaternary ammonium salt monomer, preparing method thereof and association polymer
A technology of quaternary ammonium salt monomer and long-chain alkyl, which is applied in its preparation method and associative polymer, and the field of long-chain alkyl quaternary ammonium salt monomer, which can solve the problems of limited oil reservoirs, poor viscosity-increasing performance, and salt resistance. gender issues
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[0040] The present invention also provides a kind of preparation method of long chain alkyl quaternary ammonium salt monomer, comprises the following steps:
[0041] A) reacting acryloyl chloride and the compound shown in formula 2 to obtain the compound shown in formula 3;
[0042]
[0043] B) reacting the compound shown in formula 3 obtained in the step A) with the halogenated hydrocarbon RX to obtain the long-chain alkyl quaternary ammonium salt monomer shown in formula 1;
[0044]
[0045] In formula 1, R 1 is an arylene group, R is a C8-C20 alkyl group, and X is a halogen.
[0046]
[0047] In the present invention, the reaction of step A) is preferably carried out according to the reaction equation shown in formula 7. In the present invention, the compound shown in formula 3 is obtained by mixing acryloyl chloride and the compound shown in formula 2 in a solvent for reaction. In the present invention, preferably, the compound shown in formula 2 and acryloyl ch...
Embodiment 1
[0071] The synthesis of embodiment 1.(4-acrylamido) phenyl dodecyl dimethyl ammonium bromide
[0072] Step 1: In a four-neck flask equipped with a stirrer, a thermometer, a reflux condenser, a constant pressure dropping funnel, and a nitrogen protection device, follow n(N,N-dimethyl-p-phenylenediamine): n(dimethyl Formamide (DMF)=1:2, add 102.5g N,N-dimethyl-p-phenylenediamine and 110.09gDMF, then add 15.0g sodium carbonate powder (as an acid-binding agent, react with HCl, one of the products, to promote the positive reaction ), under stirring conditions, the temperature of the system is controlled by an ice-water bath at -5~5°C, according to n(N,N-dimethyl-p-phenylenediamine):n(acryloyl chloride)=1:1.2, using constant pressure drop Slowly add the acryloyl chloride solution consisting of 81.77g of acryloyl chloride and 66.05g of DMF solvent into the liquid funnel, the molar ratio of the two is 1:1. After the addition is completed, continue to react for 4-8 hours, and after fil...
Embodiment 2
[0078] Embodiment 2. (4-acrylamido) the synthesis of phenyl dodecyl dimethyl ammonium chloride
[0079] Step 1 is the same as Example 1
[0080] Step 2: In a four-necked flask equipped with a stirrer, a thermometer, a reflux condenser, a constant pressure dropping funnel, and a nitrogen protection device, follow n (intermediate product): n (ethyl acetate): n (chlorododecane )=1:2.5:1.2, add 109.54g intermediate product, 126.86g ethyl acetate, 154.12g chlorododecane successively, pass into N2 protection, under stirring condition, temperature rises to 65 ℃, constant temperature reaction 36h, pass The solvent ethyl acetate was removed by a rotary evaporator to obtain a slightly yellow viscous liquid, which was stored in a refrigerator to form a light yellow solid, which was washed 2 to 3 times with ether, and the product was dried in a vacuum oven at 60°C for 8 hours to obtain 189.02g of (4-acrylamido) phenyl dodecyl dimethyl ammonium chloride, as shown in formula 1-2, yield 83....
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