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Aluminum(III) Chloride → 6-Hydroxy-8-methyl-1,2,3,4-tetrahydroquinolin-2-one

HRID 1913895
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1913895
Cl[CH2:2][CH2:3][C:4]([NH:6][C:7]1[CH:12]=[CH:11][C:10]([O:13]C)=[CH:9][C:8]=1[CH3:15])=[O:5].[Cl-].[Al+3].[Cl-].[Cl-]>CCCCCCC.C(Cl)(Cl)Cl>[OH:13][C:10]1[CH:11]=[C:12]2[C:7](=[C:8]([CH3:15])[CH:9]=1)[NH:6][C:4](=[O:5])[CH2:3][CH2:2]2
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 6451240Aluminum(III) ChlorideHCID 171269343-Chloro-N-(4-methoxy-2-methylphenyl)propanamide

Produkt 1

HCID 666816546-Hydroxy-8-methyl-1,2,3,4-tetrahydroquinolin-2-oneAusbeute 42,7 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6212ChloroformLösungsmittelHCID 8900HeptaneLösungsmittel

Reaktionsbedingungen

Temperatur
110 °C

Versuchsvorschrift

A suspension of 3-chloro-N-(4-methoxy-2-methylphenyl)propaneamide (0.50 g, synthesized from 3-chlorobutyryl chloride and 4-methoxy-2-methylaniline) and aluminum chloride (1.4 g) in n-heptane (4.0 mL) was stirred at 110° C. for 4 days. The reaction mixture was diluted with chloroform, followed by addition of ice-cold water under ice cooling. After stirring at room temperature for 1 hour, the organic layer and the aqueous layer were separated. The aqueous layer was extracted with ethyl acetate, and the organic layers were combined, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluting solvent: chloroform/methanol=10/0 to 97/3) to give the titled compound (0.166 g, 39%) as a light-brown solid.

Aufarbeitung

  1. additionfollowed by addition of ice-cold water under ice cooling
  2. stirringAfter stirring at room temperature for 1 hour
  3. customthe organic layer and the aqueous layer were separated
  4. extractionThe aqueous layer was extracted with ethyl acetate
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe resulting residue was purified by silica gel column chromatography (eluting solvent: chloroform/methanol=10/0 to 97/3)

Quellen und Nachweise

ORD-Eintrag
ord-cf0da3ed1b7f49408c509085dec0093d
Quelldatensatz
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08609847B2

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