StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Dimethylformamide → HCID 22493595, Verbindung

HRID 1263459
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1263459
P(Cl)(Cl)(Cl)=O.CN(C)[CH:8]=[O:9].[CH3:11][CH:12]1[CH2:21][CH2:20][CH:19]([CH3:22])[C:18]2[N:17]=[CH:16][CH:15]=[CH:14][C:13]1=2.C(=O)(O)[O-].[Na+]>C(OCC)(=O)C.CCCCCC>[CH3:11][CH:12]1[CH2:21][CH2:20][CH:19]([CH3:22])[C:18]2[NH:17][CH:16]([CH:8]=[O:9])[CH:15]=[CH:14][C:13]1=2
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 6228DimethylformamideHCID 24813Phosphorus oxychlorideHCID 516892Sodium BicarbonateHCID 22493534HCID 22493534, Verbindung

Produkt 1

HCID 22493595HCID 22493595, VerbindungAusbeute 59,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 21226206
Ethyl acetate hexane
Lösungsmittel

Versuchsvorschrift

Phosphorus oxychloride (18.6 g, 0.12 mol) was added dropwise to 29.2 g (0.4 mol) of N,N-dimethylformamide under ice cooling. After stirring at room temperature for 30 minutes, the reaction mixture was cooled over ice bath, followed by the dropwise addition of 17.0 g (0.1 mol) of 5,8-dimethyl-5,6,7,8-tetrahydroquinoline. After stirring at room temperature for one hour, the reaction mixture was poured into ice water and neutralized with an aqueous solution of sodium bicarbonate, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue so obtained was subjected to chromatography on a silica gel column (developing solvent: 10% ethyl acetate/n-hexane), whereby 11.4 g of the title compound were obtained in the form of a reddish brown oil.

Aufarbeitung

  1. temperaturethe reaction mixture was cooled over ice bath
  2. stirringAfter stirring at room temperature for one hour
  3. extractionfollowed by extraction with ethyl acetate
  4. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue so obtained

Quellen und Nachweise

ORD-Eintrag
ord-66c4e6f87e404c30a01835f3671c2bfa
Quelldatensatz
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06541474B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion