Quinoline derivatives, preparation method and application thereof, and corrosion and scale inhibitor composition
A technology of corrosion and scale inhibitor and derivatives, which can be used in drilling compositions, chemical instruments and methods, and earth-moving drilling, etc. Degradation, excellent corrosion and scale inhibition effect
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Embodiment 1
[0046] This example was used to prepare 2-methyl-5-polyoxyethylene-quinoline.
[0047] Add 19.2g of 2-methyl-5-hydroxyquinoline (chemical reagent, TCI (Shanghai) Chemical Industry Development Co., Ltd.), catalyst (sodium hydroxide, 0.1 g) into the reactor, close the reactor, and replace with nitrogen Air in the kettle, stirring, heating up to 120° C., slowly press in about 44 grams of ethylene oxide, and then continue the reaction for two hours. Cool down to get the product. NMR 13 The analysis results of C showed that the peaks with chemical shifts of 67-72 were the formed ether bonds.
Embodiment 2
[0049] This example was used to prepare 3-methyl-6-polyoxyethylene-quinoline.
[0050] Add 19.2g of 3-methyl-6-hydroxyquinoline (chemical reagent, TCI (Shanghai) Chemical Industry Development Co., Ltd.), catalyst (sodium hydroxide, 0.1 g) into the reactor, close the reactor, and replace with nitrogen Air in the kettle, stirring, heating up to 120°C, slowly press in about 27 grams of ethylene oxide, and then continue the reaction for two hours. Cool down to get the product. NMR 13 The analysis results of C showed that the peaks with chemical shifts of 67-72 were the formed ether bonds.
Embodiment 3
[0052] This example was used to prepare 4-methyl-7-polyoxyethylene-quinoline.
[0053] Add 19.2g of 4-methyl-7-hydroxyquinoline (chemical reagent, TCI (Shanghai) Chemical Industry Development Co., Ltd.), catalyst (sodium hydroxide, 0.1 g) into the reactor, close the reactor, and replace with nitrogen Air in the kettle, stirring, heating up to 120°C, slowly press in about 88 grams of ethylene oxide, and then continue the reaction for two hours. Cool down to get the product. NMR 13 The analysis results of C showed that the peaks with chemical shifts of 67-72 were the formed ether bonds.
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