Green Processing and Synthesis (Jan 2019)

An environmentally friendly acylation reaction of 2-methylnaphthalene in solvent-free condition in a micro-channel reactor

  • Li Wenpeng,
  • Jin Haibo,
  • Yang Suohe,
  • Guo Xiaoyan,
  • He Guangxiang,
  • Zhang Rongyue

DOI
https://doi.org/10.1515/gps-2019-0015
Journal volume & issue
Vol. 8, no. 1
pp. 474 – 479

Abstract

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An efficient and solvent-free acylation of 2-methylnaphthalene (2-MN) is presented using acid chloride as both the acylating agent and solvent in a micro channel reactor. The effect of the catalyst, reactant ratio, mixing temperature, reaction temperature and reaction time on the product yield and selectivity was investigated. At room temperature with a reaction time of only 15 min, the target product, 2-methyl-6-propionylnaphthalene (2,6-MPN), was obtained in 72.3% yield with 73.8% selectivity, and 2-methyl-6-acetylnaphthalene (2,6-MAN) was obtained in 54.1% yield with 55.4% selectivity. The route of synthesis provides a more environmentally friendly and efficient method to prepare 2,6-MPN with no other toxic solvents and efficient mass transfer and heat transfer.

Keywords