Water → 1-{6-[Ethyl-(2-hydroxylethyl)-amino]-2-naphthyl}ethanone

HRID 650448

Reaktionsgleichung

Reaktionsgleichung von HRID 650448
O[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([C:12](=[O:14])[CH3:13])[CH:6]=[CH:5]2.[CH2:15]([NH:17][CH2:18][CH2:19][OH:20])[CH3:16].O>C(OCC)(=O)C>[CH2:15]([N:17]([CH2:18][CH2:19][OH:20])[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([C:12](=[O:14])[CH3:13])[CH:6]=[CH:5]2)[CH3:16]

Komponenten

5

Edukt 3

HCID 962Water2×HCID 80722-(Ethylamino)ethanolHCID 826311-(6-Hydroxy-2-naphthyl)ethan-1-one

Produkt 1

HCID 153748091-{6-[Ethyl-(2-hydroxylethyl)-amino]-2-naphthyl}ethanoneAusbeute 12 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

A mixture of 1-(6-hydroxy-2-naphthyl)ethanone (744 mg, 3.92 mmol), sodium hydrogen sulfate(IV) (1.66 g, 16 mmol), 2-ethylaminoethanol (2 mL) and water (5 mL) was heated in a steel bomb at 130-140° C. for 3 days. After cooling, the mixture was distributed between water and ethyl acetate, and the organic layer was washed with brine, dried and evaporated. The residue was dissolved in acetone and loaded onto a 4 mm dry silica plate for radial chromatography. The plate was eluted with a 1:1 mixture of petroleum ether and ethyl acetate. Appropriate fractions were collected and evaporated to give 125 mg (12%)of 1-{6-[ethyl-(2-hydroxylethyl)-amino]-2-naphthyl}ethanone.

Aufarbeitung

  1. temperatureAfter cooling
  2. washthe organic layer was washed with brine
  3. customdried
  4. customevaporated
  5. dissolutionThe residue was dissolved in acetone
  6. washThe plate was eluted with a 1:1 mixture of petroleum ether and ethyl acetate
  7. customAppropriate fractions were collected
  8. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-bcb23e5dc3d3481cac2271ee18bc2af5
Quelldatensatz
uspto-grants-2001_08
Patentnummer
US06274119B1

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