Welcome to Chemistry and Industry of Forest Products,

›› 2006, Vol. 26 ›› Issue (3): 27-30.

• 研究报告 • Previous Articles     Next Articles

Study on Synthesis of p-Isopropylbenzoic Acid from β-Pinene

JIN Jian-zhong1,2, HA Cheng-yong2   

  1. 1. College of Biological and Environmental Engineering, Zhejiang Shuren University, Hangzhou 310015, China;2. Guangzhou Institute of Chemistry, Chinese Academy of Sciences, Guangzhou 510650, China
  • Received:2005-04-25 Revised:1900-01-01 Online:2006-09-30 Published:2006-09-30

Abstract: p-Isopropylbenzoic acid is synthesized from β-pinene, through a three-step sequence of oxidation, ring-opening and dehydrogenation. The overall yield is 29.9%. The synthesis of the goal is a new approach. Besides, the conditions of each reaction step are studied. The dehydrogenation of dihydrocumic acid has been discussed emphatically. The optimum conditions of dehydrogenation are 7.5% Pd/C as catalyst, p-isopropylmethylbenzene as solvent, refluxing time 2 h. The yield is 89%.

Key words: β-pinene, nopinic acid, dihydrocumic acid, p-isopropylbenzoic acid

CLC Number: