Chem. J. Chinese Universities ›› 2010, Vol. 31 ›› Issue (3): 520.

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Relationship of the Esterify Reaction Condition of 2,3,4-Trihydroxybenzophenone and 2,1-Diazonaphthaquinone-5-Sulfonyl Chloride and the Solubility of Its Product

LIU Lu, ZOU Ying-Quan*   

  1. College of Chemistry, Beijing Normal University, Beijing 100875, China
  • Received:2009-09-07 Online:2010-03-10 Published:2010-03-10
  • Contact: ZOU Ying-Quan. E-mail: zouyq@bnu.edu.cn
  • Supported by:

    深圳市容大电子材料有限公司资助.

Abstract:

The esterify product of 2,3,4-trihydroxybenzophenone and 2,1-diazonaphthaquinone-5-sulfonyl chloride is widely used as the photoactive compound in photoresist. And its solubility is the critical factor in practical production. In this paper, several 2,3,4-trihydroxybenzophenone esterify 2,1-diazonaphthaquinone-5-sulfonyl chloride photoactive compounds were synthesized at different conditions and their solubility were different. High-pressure liquid chromatography was used to determine the retention time and integral area ratio of every esterified production. And through analyzing the stable configuration of photoactive compounds, the existence of triethylamine salt of diesterified product was thought to be the main factor that affects the solubility. Above all, the optimum synthetic condition of the photoactive compound is that acetone/water(85∶15, volume ratio) is applied as the solvent and Et3N is applied as the catalyst.

Key words: 2,3,4-Trihydroxybenzophenone; Diazonaphthaquinone photoactive compound; Solubility of photoactive compound

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