Реакция #1106613

ord-390cbfb13a4b4ad39385d9afed975b43

Уравнение реакции

O=Cc1c(O)ccc2ccccc12
2-hydroxy-1-naphthaldehyde
CCO
ethanol
Cc1ccccc1N
o-toluidine
CC1(O)C=CC=CC1N=Cc1cccc2ccccc12
2-hydroxy-1-naphthylmethylidene-2-methylaniline

Реагенты

Нет

Условия реакции

Температура
70°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураunder heating
  2. 2
    КонцентрированиеThe solution was concentrated with an evaporator to about 30 ml, whereupon a crystal
  3. 3
    Другоеwas formed
  4. 4
    Фильтрацияwhich was filtered by Kiriyama funnel
  5. 5
    ДругоеDrying under reduced pressure at 25° C. for 24 hours

Методика

3.44 g (20.0 mmol) of 2-hydroxy-1-naphthaldehyde was dissolved in 50 ml ethanol under heating, and 2.14 g (20.0 mmol) of o-toluidine was added. After stirring under reflux at 70° C. for 1 hour, completion of the reaction was confirmed by TLC. The solution was concentrated with an evaporator to about 30 ml, whereupon a crystal was formed, which was filtered by Kiriyama funnel. Drying under reduced pressure at 25° C. for 24 hours gave 2-hydroxy-1-naphthylmethylidene-2-methylaniline (hereinafter, also referred to as “HNOT”) as a yellow crystal (4.24 g, 81%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08715523B2uspto-grants-2014_05