Реакция #1106615

ord-d36ce22a7706466c850f10806f51a16c

Уравнение реакции

O=Cc1c(O)ccc2ccccc12
2-hydroxy-1-naphthaldehyde
CCO
ethanol
Nc1ccccc1
aniline
Oc1ccccc1N=Cc1cccc2ccccc12
2-hydroxy-1-naphthylmethylidene aniline

Реагенты

Нет

Условия реакции

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

Обработка

  1. 1
    Температураunder heating
  2. 2
    workup.WAITUpon being left at rest over night in the refrigerator
  3. 3
    Другоеa crystal was formed
  4. 4
    Другоеthe resulting precipitation
  5. 5
    Фильтрацияwas filtered by Kiriyama funnel
  6. 6
    ДругоеDrying under reduced pressure at 25° C. for 24 hours

Методика

6.88 g (40.0 mmol) of 2-hydroxy-1-naphthaldehyde was dissolved in 10 ml ethanol under heating, and 3.72 g (40.00 mmol) of aniline was added. After stirring under reflux at 70° C. for 1 hour, completion of the reaction was confirmed by TLC. Upon being left at rest over night in the refrigerator, a crystal was formed, and the resulting precipitation was filtered by Kiriyama funnel. Drying under reduced pressure at 25° C. for 24 hours gave 2-hydroxy-1-naphthylmethylidene aniline (hereinafter, also referred to as “HNA”) as a yellow crystal (9.17 g, 93%).

Источник

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