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2,5-Dimethylphenol → HCID 24623396, Verbindung

HRID 1023528
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1023528
Cl[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][N:3]=1.[CH3:11][C:12]1[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][C:13]=1[OH:19].C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[CH3:11][C:12]1[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][C:13]=1[O:19][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][N:3]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 72672,5-DimethylphenolHCID 11430Potassium CarbonateHCID 783082-Chloro-5-nitropyridine

Produkt 1

HCID 24623396HCID 24623396, VerbindungAusbeute 90,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
110 °C

Versuchsvorschrift

In a microwave vial, 2-chloro-5-nitropyridine (80 mg, 0.505 mmol) was dissolved in 2 mL of dry dimethylformamide. 2,5-dimethylphenol (80 mg, 0.505 mmol, 1 equiv) and potassium carbonate (418 mg, 3.03 mmol, 6 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 (5 mL). The volatiles were evaporated. The residue was dissolved in dichoromethane (10 mL) and brine was added (10 mL). The organic layer was extracted 2 times with dichloromethane (2×15 mL) and 2 times with ethylacetate (2×15 mL). The organic phase was dried over sodium sulphate. The solvent was removed to afford the title compound (112 mg)

Aufarbeitung

  1. filtrationThe reaction mixture was filtered
  2. washThe filtrated solid was washed with dichloromethane (5 mL)
  3. customThe volatiles were evaporated
  4. dissolutionThe residue was dissolved in dichoromethane (10 mL)
  5. additionbrine was added (10 mL)
  6. extractionThe organic layer was extracted 2 times with dichloromethane (2×15 mL) and 2 times with ethylacetate (2×15 mL)
  7. dry with materialThe organic phase was dried over sodium sulphate
  8. customThe solvent was removed

Quellen und Nachweise

ORD-Eintrag
ord-99583c3d9d80449db6fa48897101d295
Quelldatensatz
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08722695B2

Notizen zur Reaktion

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