초록 ▼

Provided is a method for preparing 2,5-dimethylphenylacetic acid, wherein p-xylene is mixed with paraformaldehyde and concentrated hydrochloric acid in a solvent of ion liquid to obtain 2,5-dimethyl benzyl chloride by the chloromethylation reaction. Then, 2,5-dimethyl benzyl chloride is introduced i

Provided is a method for preparing 2,5-dimethylphenylacetic acid, wherein p-xylene is mixed with paraformaldehyde and concentrated hydrochloric acid in a solvent of ion liquid to obtain 2,5-dimethyl benzyl chloride by the chloromethylation reaction. Then, 2,5-dimethyl benzyl chloride is introduced into a reactor with an acid binding agent and a solvent, the carbonylation and hydrolysis reaction is conducted in the presence of a catalyst to obtain 2,5-dimethylphenylacetic acid. The present process has new route, less synthesis steps, simple operation, lower cost, increased yield, and is friendly to the environment. Therefore, the method is suitable for industrial production.

대표청구항 ▼

1. A method for preparing 2,5-dimethylphenylacetic acid, comprising: (1) producing 2,5-dimethylbenzyl chloride by performing a chloromethylation reaction comprising the following steps: mixing together p-xylene, a solvent ionic liquid, paraformaldehyde, and concentrated hydrochloric acid to obtain a

1. A method for preparing 2,5-dimethylphenylacetic acid, comprising: (1) producing 2,5-dimethylbenzyl chloride by performing a chloromethylation reaction comprising the following steps: mixing together p-xylene, a solvent ionic liquid, paraformaldehyde, and concentrated hydrochloric acid to obtain a first reaction mixture, wherein the mole ratio of the p-xylene, paraformaldehyde, and ionic liquid is 1:1.1-5:0.01-1;heating the first reaction mixture to a predetermined temperature;contacting the first reaction mixture with hydrogen chloride gas and allowing the chloromethylation reaction to proceed;maintaining the temperature of the reaction mixture at the predetermined temperature until 30 minutes after the reaction is completed;cooling the chloromethylation reaction solution, and allowing the reaction solution to layer into an organic layer and a water layer; andrectifying the organic layer under vacuum to obtain 2,5-dimethylbenzyl chloride; and(2) subjecting 2,5-dimethylbenzyl chloride to carbonylation and hydrolyzation reactions, comprising the following steps: adding to a reactor the 2,5-dimethylbenzyl chloride obtained from the chloromethylation reaction, an acid binding agent, and a catalyst to obtain a second reaction mixture;heating the second reaction mixture to a predetermined temperature;contacting the second reaction mixture with carbon monoxide gas and allowing the carbonylation and hydrolvzation reactions to proceed;after the reactions are completed, cooling the carbonylation and hydrolyzation reaction solution; and thenadding liquid caustic soda to the cooled solution under a nitrogen atmosphere, and stirring;allowing the reaction solution to layer into an organic layer and a water layer;adjusting the pH of the water layer to a pH of 1; and thenfiltering the reaction solution to obtain 2,5-dimethylphenylacetic acid. 2. The method according to claim 1, wherein: in the chloromethylation reaction, the mole ratio of p-xylene, paraformaldehyde and ionic liquid is 1:1.1-2.0:0.01-0.5;in the chloromethylation reaction, the solvent is a substituted imidazole ionic liquid comprising an imidazole cation, and an anion selected from halogen ion, trifluoromethanesulfonate ion, tetrafluoroborate ion, and hexafluorophosphate ion;in the carbonylation and hydrolyzation reactions, the catalyst is selected from the group consisting of palladium chloride, palladium acetate, palladium sulfate, palladium nitrate, palladium oxide, dichlorodiamminepalladium, tetraammine dichloropalladium(II), tetrakis(triphenylphosphine)palladium(0), palladium(II)bis(triphenylphosphine) diacetate, palladium(II)bis(triphenyl- phosphine) dichloride, and palladium hydroxide;in the carbonylation and hydrolyzation reactions, the acid binding agent is selected from the group consisting of pyridine, triethylamine, alkali alcoholate, lithium alkylide, lithium amide, alkali hydroxide, alkali carbonate or bicarbonate, and acetate;in the carbonylation and hydrolyzation reactions, the solvent is selected from the group consisting of esters, ethers, alcohols, arenes, nitriles, and mixtures thereof. 3. The method according to claim 2, wherein: in the carbonylation and hydrolyzation reactions, the catalyst is tetrakis(triphenylphosphine)palladium(0), palladium(II)bis(triphenylphosphine) diacetate, or palladium(II)bis(triphenylphosphine) dichloride; andin the carbonylation and hydrolyzation reactions, the acid binding agent is pyridine or triethylamine. 4. The method according to claim 2, wherein the solvent of the carbonylation and hydrolyzation reactions is selected from the group consisting of methyl acetate, ethyl acetate, butyl acetate, ethyl ether, methyl t-butyl ether, tetrahydrofuran, p-dioxane, methanol, ethanol, isopropyl alcohol, tert-pentanol, benzene, toluene, chlorobenzene, acetonitrile, and propionitrile. 5. The method according to claim 4, wherein the solvent of the carbonylation and hydrolyzation reactions is isopropyl alcohol or tert-pentanol. 6. The method according to claim 1, further comprising: recovering the ionic liquid by dehydrating the water layer obtained from the chloromethylation reaction under vacuum so that the ionic liquid may be recycled and reused. 7. The method according to claim 1, further comprising: recovering the catalyst used in the carbonylation and hydrolyzation reactions by adding heavy metal capture agent and flocculant to a filtrate obtained in the filtering step, and refiltering the filtrate so that the catalyst may be recycled and reused.