Synthetic Studies of Coumarin Derivatives from o-Hydroxybenzophenones with Phenylacetic Acid and Acetic Anhydride

o-Hydroxybenzophenones와 Phenylacetic Acid, Acetic Anhydride에 의한 Coumarin 유도체 합성에 관한 연구

  • Kang, Soon Hee (Department of Science Education, College of Education, Ewha Womans University) ;
  • Yang, Sung Yun (Department of Science Education, College of Education, Ewha Womans University)
  • 강순희 (이화여자대학교 사범대학 과학교육과) ;
  • 양성윤 (이화여자대학교 사범대학 과학교육과)
  • Published : 19990200

Abstract

The 8 coumarin derivatives have been synthesized from 8 starting materials(2-hydroxy-benzophenone, 2,2'-dihydroxybenzophenone, 2,4-dihydroxybenzophenone, 2-hydroxy-5-methylbenzophenone, 5-chloro-2-hydroxy-4-methylbenzophenone, 2-hydroxy-4-methoxybenzophenone, 2-hydroxy-4-ethoxybenzophenone, 2-hydroxy-4,4'-dimethoxybenzophenone) with phenylacetic acid and $Ac_2$O/TEA in acetone at reflux temperature. The ratio of o-hydroxybenzophenone, phenylacetic acid, $Ac_2$O and TEA is 1 : 1: 8: 8 in acetone. Our results showed higher products yields of coumarin derivatives than Shama and Ray's method in previous papers. A new intermediate form was proposed to our mechanism of coumarin synthetic method.

o-Hydroxybenzophenone 유도체 (2-hydroxybenzophenone, 2,2'-dihydroxybenzo phenone, 2,4-dihydroxybenzophenone, 2-hydroxy-5-methylbenzophenone, 5-chloro-2-hydroxy-4-methylbenzophenone 2-hydroxy-4-methoxybenzophenone, 2-hydroxy-4-ethoxybenzophenone, 2-hydroxy-4,4'-dimethoxybenzophenone)들을 출발물질로 하여 8종의 coumarin 유도체들을 합성하였다. o-Hydroxybenzophenone과 같은 몰량의 phenylacetic acid를 사용하여 염기인 triethylamine(TEA)와 acetic anhydride를 o-hydroxybenzophenone에 대해 1:8의 비율로 아세톤에서 환류온도로 반응시켜 coumarin 유도체들을 합성한 경우가 가장 수득율이 좋았다. 이것은 용매로 acetic anhydride를 사용한 Sham와 Ray 방법보다 좋은 결과였다.

Keywords

References

  1. Modification of Polycyclic Aromatic Hydrocarbon carcinogenesis Digiovanni, J.;Slaga, T. J.;Gelboin, H. V.(ed.);Ts'o, P. O. P.(ed.)
  2. Ann. Biochem. Exp. Med. v.17 Chakraborty, D. P.;Das Gupta, A.;Bose, P. K.
  3. Br. J. Pharmacol. v.20 Arora, R. B.;Mathur, C. N.
  4. J. Pharm. Sci. v.51 Willwtte, R. E.;Soine, T. O.
  5. Organic Reactions v.Ⅶ Adams, R.;Blatt, A. H.
  6. Indian J. of Chem. v.I no.23B John, A. C.;Arya, P.;Nayyar, N. K.
  7. Ber v.70 Spoth, E.
  8. J. Chem. Soc. Russell;Todd;Wilkinson;Macdonald;Woolfe
  9. J. Am. Chem. Soc. v.63 Adams;Loewe;Jeinek;Wolff
  10. Carcinogenesis v.12 Harvey, R. G.;Cortez, C.;Nair, R. V.;Safe, S. H.
  11. Tetrahedron Letters v.26 Corombie, L.;Jones, R. C. F.;Plamer, C. J.
  12. J. Org. Chem. v.56 Snieckus, V.;Alo, B. I.;Kandil, P. A.;Patil, P. A.
  13. J. of Organometallic Chem. v.371 An, Z.;Catellani, M.;Chiusoli, G. P.
  14. Indian J. of Chem. v.27B Shama, I.;Ray, S.
  15. 이화여자대학교 대학원 석사 학위 논문 정희영
  16. Org. React. v.7 Sethna, S.;Phardke, R.