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Potassium Carbonate → HCID 28254339, Verbindung

HRID 1023521
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1023521
Cl[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][N:3]=1.[CH3:11][CH:12]([C:14]1[CH:15]=[C:16]([OH:20])[CH:17]=[CH:18][CH:19]=1)[CH3:13].C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[CH3:11][CH:12]([C:14]1[CH:15]=[C:16]([O:20][C:2]2[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][N:3]=2)[CH:17]=[CH:18][CH:19]=1)[CH3:13]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 11430Potassium CarbonateHCID 120593-IsopropylphenolHCID 783082-Chloro-5-nitropyridine

Produkt 1

HCID 28254339HCID 28254339, VerbindungAusbeute 82,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
110 °C

Versuchsvorschrift

In a 30 mL large microwave vial, 2-chloro-5-nitropyridine (1.041 g, 6.57 mmol, 1 equiv) was dissolved in 5.5 mL of dimethylformamide. 3-(1-methylethyl)phenol (0.90 mL, 6.57 mmol, 1 equiv) and potassium carbonate (4.54 g, 32.8 mmol, 5 equiv) were added. The reaction mixture was heated under microwave irradiation for 1 hour at 110° C. (Biotage Initiator). The reaction mixture was filtered. The filtrated solid was washed with dichloromethane (30 mL). The volatiles were evaporated under vacuum. The crude compound was dissolved in dichoromethane (20 mL) and brine was added (20 mL). The compound was extracted 2 times with dichloromethane (2×20 mL) and 2 times with ethyl acetate (2×20 mL). The organic phase was dried over sodium sulphate. Evaporation afforded the title compound (1.402 g).

Aufarbeitung

  1. filtrationThe reaction mixture was filtered
  2. washThe filtrated solid was washed with dichloromethane (30 mL)
  3. customThe volatiles were evaporated under vacuum
  4. dissolutionThe crude compound was dissolved in dichoromethane (20 mL)
  5. additionbrine was added (20 mL)
  6. extractionThe compound was extracted 2 times with dichloromethane (2×20 mL) and 2 times with ethyl acetate (2×20 mL)
  7. dry with materialThe organic phase was dried over sodium sulphate
  8. customEvaporation

Quellen und Nachweise

ORD-Eintrag
ord-b1312467dc74472bb4c9d8df85791c4f
Quelldatensatz
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08722695B2

Notizen zur Reaktion

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