Hydroquinone Carbozylation to 2,5-dihydrozyterephthalic Acid by Solvent Method and the Activity of PdCl2/C Catalyst
1.Introduction 2,5-Dihydroxyterephthalic acid (2,5-DHTA) is an important intermediate in organic synthesis, which is widely used for the manufacture of organic optoelectronic materials, colorants, and fluorescent materials. 2,5-DHTA can react with glycols for the manufacture of linear polyester and copolyesters possessing fiber-or film-forming properties1-3. The synthesis of 2,5-DHTA can be carried out by a Kolbe-Schmitt reaction. The Kolbe-Schmitt reaction involves three steps, which are shown in Scheme 1.Potassium salt of hydroquinone is first prepared by reaction of hydroquinone with potassium hydroxide or potassium carbonate. The second step is the carboxylation of dipotassium salt of hydroquinone with CO2 under high pressure. Then 2,5-DHTA can be obtained by acidification with hydrochloric acid.
2,5-Dihydrozyterephthalic acid Solvent method PdCl2/C catalyst Hydroquinone
Lin Qi Hengbo Yin Yutang Shen Huihong Lu Tingshun Jiang Longbao Yu
Faculty of Chemistry and Chemical Engineering,Jiangsu University,Zhenjiang 212013,China
国际会议
江苏镇江
英文
60-61
2008-10-15(万方平台首次上网日期,不代表论文的发表时间)