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Ammonium Chloride → 1-[1-(1-Methylethyl)-1,2,3,4-tetrahydroquinolin-6-yl]ethanol

HRID 2229167
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2229167
[CH3:1][Mg]Br.[CH3:4][CH:5]([N:7]1[C:16]2[C:11](=[CH:12][C:13]([CH:17]=[O:18])=[CH:14][CH:15]=2)[CH2:10][CH2:9][CH2:8]1)[CH3:6].[Cl-].[NH4+]>CCOCC>[CH3:6][CH:5]([N:7]1[C:16]2[C:11](=[CH:12][C:13]([CH:17]([OH:18])[CH3:1])=[CH:14][CH:15]=2)[CH2:10][CH2:9][CH2:8]1)[CH3:4]
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Komponenten

5

Edukt 3

HCID 25517Ammonium ChlorideHCID 31574891-Isopropyl-1,2,3,4-tetrahydro-quinoline-6-carbaldehydeHCID 178418573HCID 178418573, Verbindung

Produkt 1

HCID 106089181-[1-(1-Methylethyl)-1,2,3,4-tetrahydroquinolin-6-yl]ethanol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

4.9 ml (15 mmol) of a 3.0M ethereal solution of methylmagnesium bromide was diluted with 15 ml of ether. An ethereal solution of 2.0 g (10 mmol) of 1-(1-methylethyl)-1,2,3,4-tetrahydroquinoline-6-carbaldehyde was dropped into the dilution prepared above at room temperature. The obtained mixture was stirred at room temperature for one hour, followed by the addition of an aqueous solution of ammonium chloride. The resulting mixture was extracted with ethyl acetate. The organic phase was washed with a saturated aqueous solution of common salt, dried over anhydrous magnesium sulfate and concentrated in a vacuum to give 2.1 g of the title compound as a brown oil.

Aufarbeitung

  1. customprepared above at room temperature
  2. extractionThe resulting mixture was extracted with ethyl acetate
  3. washThe organic phase was washed with a saturated aqueous solution of common salt
  4. dry with materialdried over anhydrous magnesium sulfate
  5. concentrationconcentrated in a vacuum

Quellen und Nachweise

ORD-Eintrag
ord-2cdbacd29c21476aa6789a4bd5b15cb3
Quelldatensatz
uspto-grants-2002_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06420363B1

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