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Dimethylformamide → 2-Formyl-3-methyl-5-(4-methylphenyl)furan

HRID 22245
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 22245
P(Cl)(Cl)(Cl)=O.CN(C)[CH:8]=[O:9].[CH3:11][C:12]1[CH:16]=[C:15]([C:17]2[CH:22]=[CH:21][C:20]([CH3:23])=[CH:19][CH:18]=2)[O:14][CH:13]=1.[OH-].[Na+]>ClC(Cl)C>[CH:8]([C:13]1[O:14][C:15]([C:17]2[CH:22]=[CH:21][C:20]([CH3:23])=[CH:19][CH:18]=2)=[CH:16][C:12]=1[CH3:11])=[O:9]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 6228DimethylformamideHCID 14798Sodium HydroxideHCID 24813Phosphorus oxychlorideHCID 13926387HCID 13926387, Verbindung

Produkt 1

HCID 194301992-Formyl-3-methyl-5-(4-methylphenyl)furan

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6365
1,1-Dichloroethane
Lösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Phosphorus oxychloride (12 ml) was added slowly to dimethylformamide (9.85 ml) with stirring at 0° C., and the mixture stirred at 0° C. for 30 minutes. A solution of 3-methyl-5-(4-methylphenyl)furan (22 g) in 50 ml of dichloroethane was added dropwise over a period of 15 minutes, maintaining the temperature at 0° C. The mixture was then stirred at room temperature for 11/2 hours. Ice water was then added, and the pH of the aqueous layer adjusted to about 8 with dilute sodium hydroxide. The organic layer was separated, the aqueous layer extracted with dichloromethane, the organic portions combined and solvent removed under reduced pressure. The solvent was removed from the filtrate under reduced pressure, and the residue flash chromatographed on silica gel, eluting with 10% ethyl acetate in heptane, to yield 19.2 g of 2-formyl-3-methyl-5-(4-methylphenyl)furan.

Aufarbeitung

  1. stirringthe mixture stirred at 0° C. for 30 minutes
  2. temperaturemaintaining the temperature at 0° C
  3. stirringThe mixture was then stirred at room temperature for 11/2 hours
  4. customThe organic layer was separated
  5. extractionthe aqueous layer extracted with dichloromethane
  6. customsolvent removed under reduced pressure
  7. customThe solvent was removed from the filtrate under reduced pressure
  8. customthe residue flash chromatographed on silica gel
  9. washeluting with 10% ethyl acetate in heptane

Quellen und Nachweise

ORD-Eintrag
ord-1d5091b33d1b49e295010bdab9394b2a
Quelldatensatz
uspto-grants-1995_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05428037

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