Synthesis of 6-benzoyl-2(3H)-benzoxazolone and 6-benzoyl-2(3H)-benzothiazolone

Ucar, H;Vanderpoorten, K;Kanyonyo, M;Isa, M.;Poupaert, Jacques;et.al.
(1996) Societes Chimiques Belges. Bulletin — Vol. 105, n° 12, p. 773-776 (1996)

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  • Ucar, H
    Author
  • Vanderpoorten, K
    Author
  • Kanyonyo, M
    Author
  • Isa, M.
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  • Poupaert, JacquesUCLouvain
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Abstract
This paper reports and compares different methods to synthesize 6-benzoyl-2(3H)-benzoxazolone and 6-benzoyl-2(3H)-benzothiazolone by Fridel-Crafts acylation of 2(3H)-benzoxazolone and 2(3H)-benzothiazolone. The best method found consisted of the transposition of the N-benzoyl derivative fa the target compound, a process taking place at 160 degrees C and catalyzed by AlCl3. In these conditions, 6-benzoyl-2(3H)-benzoxazolone and 6-benzoyl-2(3H)-benzothiazolone were obtained in 80 and 85 % yield, respectively.
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Ucar, H., Vanderpoorten, K., Kanyonyo, M., Isa, M., Lambert, D., Lesieur, D., & Poupaert, J. (1996). Synthesis of 6-benzoyl-2(3H)-benzoxazolone and 6-benzoyl-2(3H)-benzothiazolone. Societes Chimiques Belges. Bulletin, 105(12), 773-776. https://hdl.handle.net/2078.5/246898 (Original work published 1996)