Реакция #740410

ord-d40068c51f3f4e71b8bf550b2095608a

Уравнение реакции

CC(=O)Oc1ccccc1
phenyl acetate
O=C(CO)c1ccccc1
2-hydroxyacetophenone
CC(=O)c1ccc(O)cc1
4-hydroxyacetophenone
COc1ccccc1OC(C)=O
guaiacol acetate
CC(=O)Oc1cccc(C)c1
m-cresyl acetate
CC(=O)Oc1ccc(C)cc1
p-cresyl acetate

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеwith a maximum yield of 81% after 24 hours of reaction time
  2. 2
    Другоеto be obtained by K
  3. 3
    Другоеin yields may

Методика

Dann and Mylius in a dissertation included as part of a series of Reports from the Institute for Applied Chemistry of the University of Erlangen, received for publication on Jan. 7, 1954 and published in Annalen der Chemie 587 Band, pages 1 to 15, show the rearrangement of phenyl acetate in hydrogen fluoride to 4-hydroxyacetophenone, with a maximum yield of 81% after 24 hours of reaction time. They also report a yield of 92% from this reaction stated to be obtained by K. Weichert as reported in Angewandte Chemie 56, 338 (1943), but suggest that the difference in yields may be at least partly due to the previous ignoring by Weichert of the accompanying 2-hydroxyacetophenone. Dann and Mylius also report somewhat lower yields of hydroxy aromatic ketones from rearrangements in hydrogen fluoride of m-cresyl acetate, p-cresyl acetate, and guaiacol acetate.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04675449uspto-grants-1987_06