Реакция #155310

ord-531862ea724b4025a6820c232ec276a5

Уравнение реакции

CCCOc1cc2ccccc2cc1NC(C)=O
N-(3-Propoxynaphthalen-2-yl)acetamide
Cl
hydrochloric acid
[Na+].[OH-]
sodium hydroxide
CCCOc1cc2ccccc2cc1N
3-propoxynaphthalen-2-ylamine
Выход 100.0%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураwhile heating
  2. 2
    Температураunder reflux
  3. 3
    Экстракцияfollowed by extraction
  4. 4
    КонцентрированиеThe thus-obtained organic layer was concentrated to dryness under reduced pressure
  5. 5
    Другоеthe residue was then purified
  6. 6
    КонцентрированиеThe purified product was concentrated to dryness under reduced pressure

Методика

N-(3-Propoxynaphthalen-2-yl)acetamide (2.5 g, 10.2 mmol) was dissolved in ethanol (10 ml). Concentrated hydrochloric acid (5.2 ml) was added thereto, and the resulting mixture was stirred for 4 hours while heating under reflux. The reaction mixture was cooled to room temperature, and a 5N aqueous sodium hydroxide solution (12.5 ml) was added thereto to adjust its pH to 11, followed by extraction using dichloromethane. The thus-obtained organic layer was concentrated to dryness under reduced pressure, and the residue was then purified using silica gel column chromatography (dichloromethane). The purified product was concentrated to dryness under reduced pressure, giving a white powder of 3-propoxynaphthalen-2-ylamine (2.05 g, yield: 100%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: USRE045108E1uspto-grants-2014_09