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Sodium Hydroxide → 3-[2-(N,N-Dimethylamino)ethyl]-1,2,3,4-tetrahydroquinoline

HRID 2269714
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2269714
[CH3:1][N:2]([CH3:17])[C:3](=O)[CH2:4][CH:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[NH:7][C:6]1=O.[OH-].[Na+]>Cl>[CH3:1][N:2]([CH2:3][CH2:4][CH:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[NH:7][CH2:6]1)[CH3:17]
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Komponenten

4

Edukt 2

HCID 14798Sodium HydroxideHCID 10585665N,N-Dimethyl-2-oxo-1,2,3,4-tetrahydro-3-quinolineacetoamide

Produkt 1

HCID 183331263-[2-(N,N-Dimethylamino)ethyl]-1,2,3,4-tetrahydroquinolineAusbeute 75,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 313Hydrochloric AcidLösungsmittel

Versuchsvorschrift

Borane-THF complex (1M; 15 ml) was added to N,N-dimethyl-2-oxo-1,2,3,4-tetrahydro-3-quinolineacetoamide (590 mg), which was heated under reflux for 3.5 hours. 6N hydrochloric acid (10 ml) was added to the reaction mixture, which was heated under reflux overnight. 6N sodium hydroxide was added to the reaction mixture to adjust pH to 7 and extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium bicarbonate solution and a saturated aqueous sodium chloride solution, then dried and concentrated. The residue was purified by alumina column chromatography (eluent: hexane/ethyl acetate=1/1) to obtain the entitled compound (390 mg) as an oily substance.

Aufarbeitung

  1. temperaturewas heated
  2. temperatureunder reflux for 3.5 hours
  3. temperaturewas heated
  4. temperatureunder reflux overnight
  5. extractionextracted with ethyl acetate
  6. washThe organic layer was washed with a saturated aqueous sodium bicarbonate solution
  7. dry with materiala saturated aqueous sodium chloride solution, then dried
  8. concentrationconcentrated
  9. customThe residue was purified by alumina column chromatography (eluent: hexane/ethyl acetate=1/1)

Quellen und Nachweise

ORD-Eintrag
ord-5e6b2901d14c47e4aba22c49b92f3992
Quelldatensatz
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06329389B1

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