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Ethanol → 2-(2-Aminoethoxy)naphthalene

HRID 518944
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 518944
O.[OH-].[Ba+2].[OH-].C(O)C.[CH:8]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH:11]=[CH:10][C:9]=1[O:18][CH2:19][CH2:20][NH:21]C(=O)C>C(OCC)(=O)C>[CH:8]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH:11]=[CH:10][C:9]=1[O:18][CH2:19][CH2:20][NH2:21]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 702EthanolHCID 962Water2×HCID 4128976N-[2-(2-naphthyloxy)ethyl]acetamideHCID 6093286Barium hydroxide

Produkt 1

HCID 27942452-(2-Aminoethoxy)naphthaleneAusbeute 103,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8857
Ethyl Acetate
Lösungsmittel

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

A 3-neck round bottom flask was charged with water (50 mL) and barium hydroxide (12.27 g, 71.61 mmol) while stirring. The resulting slurry was charged with ethanol (50 mL) and finally N-(2-(naphthalen-2-yloxy)ethyl)acetamide (10.0 g, 35.80 mmol) as prepared above. The resulting mixture was heated to reflux for 18 h. The reaction was monitored by TLC. The reaction was then allowed to cool to 50° C., then charged with water (50 mL) followed by ethyl acetate (100 mL). The mixture was then stirred for 15 min. The mixture was then filtered and thelayers were separated. The upper organic layer was washed with saturated sodium chloride (50 mL) and dried over sodium sulfate and concentrate to afford 2-(2-naphthyloxy)ethylamine as an amber oil (6.92 g, 47%).

Aufarbeitung

  1. customas prepared above
  2. temperatureThe resulting mixture was heated
  3. temperatureto reflux for 18 h
  4. stirringThe mixture was then stirred for 15 min
  5. filtrationThe mixture was then filtered
  6. customthelayers were separated
  7. washThe upper organic layer was washed with saturated sodium chloride (50 mL)
  8. dry with materialdried over sodium sulfate
  9. concentrationconcentrate

Quellen und Nachweise

ORD-Eintrag
ord-17d0ed3c05234243981bc0b3ddcb081e
Quelldatensatz
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09115237B2

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