Реакция #935343

ord-469f2215b931479dae9e1401e36ce6dc

Уравнение реакции

O=C(CO)c1ccccc1
2-hydroxyacetophenone
O=Cc1ccncc1
pyridine-4-carbaldehyde
Cl
hydrochloric acid
[Na+].[OH-]
sodium hydroxide
O=C(CC(O)c1ccncc1)c1ccccc1O
1-(2-hydroxyphenyl) 3-(4-pyridyl) 3-hydroxy 1-propanone

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.DISSOLUTIONAn abundant yellow precipitate forms at first which then gradually dissolves
  2. 2
    ДругоеThe yellow precipitate obtained
  3. 3
    Фильтрацияis filtered
  4. 4
    Промывкаwashed with water
  5. 5
    Другоеdried

Методика

According to the method of Corvaisier (Bull. Soc. Chim. Fr. 1962, 528) 15 ml of an 11 N aqueous sodium hydroxide solution are added to a solution of 24 g of 2-hydroxyacetophenone and 21 g of pyridine-4-carbaldehyde in 130 ml of absolute ethanol maintained an ambient temperature. An abundant yellow precipitate forms at first which then gradually dissolves. After two hours at ambient temperature the mixture is adjusted to pH 1 by means of hydrochloric acid. The yellow precipitate obtained is filtered, washed with water and dried. 27 g of 1-(2-hydroxyphenyl) 3-(4-pyridyl) 3-hydroxy 1-propanone melting at 150° C. are obtained.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04294841uspto-grants-1981_10