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Potassium Carbonate → 6-(4-Cyanophenoxy)-2-(4-trifluoromethoxyphenoxy)nicotinic acid ethyl ester

HRID 1024696
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1024696
C(=O)([O-])[O-].[K+].[K+].[CH2:7]([O:9][C:10](=[O:27])[C:11]1[CH:16]=[CH:15][C:14]([O:17][C:18]2[CH:23]=[CH:22][C:21]([C:24]#[N:25])=[CH:20][CH:19]=2)=[N:13][C:12]=1Cl)[CH3:8].[F:28][C:29]([F:39])([F:38])[O:30][C:31]1[CH:36]=[CH:35][C:34]([OH:37])=[CH:33][CH:32]=1>CN(C=O)C>[CH2:7]([O:9][C:10](=[O:27])[C:11]1[CH:16]=[CH:15][C:14]([O:17][C:18]2[CH:23]=[CH:22][C:21]([C:24]#[N:25])=[CH:20][CH:19]=2)=[N:13][C:12]=1[O:37][C:34]1[CH:35]=[CH:36][C:31]([O:30][C:29]([F:28])([F:38])[F:39])=[CH:32][CH:33]=1)[CH3:8]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 11430Potassium CarbonateHCID 70015p-(Trifluoromethoxy)phenolHCID 86665953HCID 86665953, Verbindung

Produkt 1

HCID 676057626-(4-Cyanophenoxy)-2-(4-trifluoromethoxyphenoxy)nicotinic acid ethyl esterAusbeute 94,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel
2×

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

Potassium carbonate (60 mg, 0.43 mmol) was added to a stirred and cooled (0° C.) solution of 2-chloro-6-(4-cyano phenoxy)nicotinic acid ethyl ester 0.13 g (0.43 mmol) in 10 ml DMF and stirred for 10 min at the same temperature. This was followed by the addition of 76.5 mg (0.43 mmol) of 4-trifluoromethoxy phenol, dissolved in 2 ml of DMF, over a period of 10 min. After the addition was completed, the contents were allowed to stir at RT. This was followed by heating for 3 h at 80° C. The reaction mixture was concentrated under reduced pressure, poured into ice-cold water and dissolved in 50 ml of ethyl acetate. Organic layer was then washed with brine solution followed by water and the crude product was purified by column chromatography using hexane:ethyl acetate (8:2) to afford 0.18 g of the required product. Percentage purity: LCMS−ve mode): 20.12%.

Aufarbeitung

  1. stirringstirred for 10 min at the same temperature
  2. additionAfter the addition
  3. stirringto stir at RT
  4. concentrationThe reaction mixture was concentrated under reduced pressure
  5. additionpoured into ice-cold water
  6. dissolutiondissolved in 50 ml of ethyl acetate
  7. washOrganic layer was then washed with brine solution
  8. customthe crude product was purified by column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-7a43184c2d8e43cc9265eef113be0a6c
Quelldatensatz
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08722930B2

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