Water → [(3-Aminobutan-2-yl)oxy]benzene

HRID 1288236Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1288236
[O:1]([CH:8]([CH3:13])[C:9](=[N:11]O)[CH3:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[OH-].[Na+]>CCOCC>[O:1]([CH:8]([CH:9]([NH2:11])[CH3:10])[CH3:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Komponenten

6

Versuchsvorschrift

A solution of 3-phenoxybutan-2-one oxime (28.8 g.) in dry ether (150 ml.) was added dropwise, over 45 minutes, to a stirred, refluxing mixture of lithium aluminium hydride (6.3 g.) in dry ether (100 ml.). Stirring and heating were continued for 4 hours and the mixture was cooled and treated cautiously with water (6.3 ml.) followed by 15% aqueous sodium hydroxide (6.3 ml.), and finally, water (18.9 ml.). The mixture was stirred for 30 minutes and then filtered. The filtrate was extracted with 2N-hydrochloric acid (150 ml.) and the acid extract was made strongly basic with sodium hydroxide and extracted with ether. The ether extract was dried over anhydrous potassium carbonate, evaporated, and distilled to give a fraction, b.p. 118°-124°/14 mm. Redistillation gave pure 2-phenoxybut-3-ylamine, b.p. 116°-118°/14 mm.

Aufarbeitung

  1. temperaturerefluxing
  2. temperatureheating
  3. temperaturethe mixture was cooled
  4. stirringThe mixture was stirred for 30 minutes
  5. filtrationfiltered
  6. extractionThe filtrate was extracted with 2N-hydrochloric acid (150 ml.)
  7. extractionthe acid extract
  8. extractionextracted with ether
  9. extractionThe ether extract
  10. dry with materialwas dried over anhydrous potassium carbonate
  11. customevaporated
  12. distillationdistilled
  13. customto give a fraction, b.p. 118°-124°/14 mm
  14. distillationRedistillation

Quellen und Nachweise

ORD-Eintrag
ord-350422bd6cb94c439794521fa9496699
Quelldatensatz
uspto-grants-1976_10
Patentnummer
US03987158

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