Ion liquid of quaternaries of naphthenic acid
A technology of ionic liquids and quaternary ammonium salts, applied in the field of chemical industry, can solve the problems of difficult purification of ionic liquid products and unfriendly environment
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Embodiment 1
[0010] Accurately weigh 2.563 g of 0.02 mol of cyclohexane carboxylic acid, put it into a round bottom flask, then add 10 ml of ethanol therein as a reaction medium, and stir sufficiently to completely dissolve the cyclohexane carboxylic acid to obtain a clear and transparent homogeneous solution. Then, under the condition of stirring, 5.246 g of 45 wt % choline solution was slowly added dropwise therein. Reaction at room temperature for 18h. The reactants were evaporated in vacuum at 50°C for 90 minutes to remove most of the ethanol, and then the obtained liquid was dried in a vacuum oven at 50°C for 48 hours to finally obtain 4.367 g of a colorless, viscous liquid product.
Embodiment 2
[0012] Accurately weigh 2.763g of salicylic acid, put it into a round bottom flask, add 10ml of ethanol therein as a reaction medium, and stir fully to completely dissolve the salicylic acid to obtain a clear and transparent homogeneous solution. Then, under the condition of stirring, 5.306 g of 45 wt % choline solution was slowly added dropwise therein. The reaction was carried out for 20 h at a temperature of 25°C. The reactant was evaporated in vacuo at 50°C for 60 minutes to remove most of the ethanol, and then the obtained liquid was dried in a vacuum oven at 50°C for 48 hours to finally obtain 4.526 g of a light yellow, viscous liquid product.
Embodiment 3
[0014] Accurately weigh 2.585 g of cyclohexane carboxylic acid, put it into a round bottom flask, then add 5 ml of methanol as the reaction medium, and stir fully to completely dissolve the cyclohexane carboxylic acid to obtain a clear and transparent homogeneous solution. Then, under the condition of stirring, 8.401 g of methanol solution of 40 wt % benzyltrimethylammonium hydroxide was slowly added dropwise thereto. Under the temperature condition of 20 ℃, react for 22h. The reactants were evaporated in vacuo at 40°C for 90 minutes to remove most of the methanol, and then the obtained product was dried in a vacuum oven at 50°C for 48 hours to finally obtain 5.210 g of the product.
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