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Ethylparaben → Ethyl 4-{[5-(trifluoromethyl)pyridin-2-yl]oxy}benzoate

HRID 230797
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 230797
C(=O)([O-])[O-].[K+].[K+].Br[C:8]1[CH:13]=[CH:12][C:11]([C:14]([F:17])([F:16])[F:15])=[CH:10][N:9]=1.[OH:18][C:19]1[CH:24]=[CH:23][C:22]([C:25]([O:27][CH2:28][CH3:29])=[O:26])=[CH:21][CH:20]=1>C(#N)C>[F:15][C:14]([F:17])([F:16])[C:11]1[CH:12]=[CH:13][C:8]([O:18][C:19]2[CH:20]=[CH:21][C:22]([C:25]([O:27][CH2:28][CH3:29])=[O:26])=[CH:23][CH:24]=2)=[N:9][CH:10]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 8434EthylparabenHCID 11430Potassium CarbonateHCID 27364342-Bromo-5-(trifluoromethyl)pyridine

Produkt 1

HCID 4271674Ethyl 4-{[5-(trifluoromethyl)pyridin-2-yl]oxy}benzoateAusbeute 79,7 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

Potassium carbonate (1.4 g) and 2-bromo-5-trifluoromethylpyridine (450 mg) were added to an acetonitrile solution (10 mL) of ethyl 4-hydroxybenzenecarboxylate (221 mg), and heated overnight under reflux. The reaction solution was concentrated under reduced pressure, water was added to the residue and extracted with ethyl acetate. The organic layer was dried with anhydrous magnesium sulfate, and the solvent was evaporated off under reduced pressure. The resulting residue was purified through silica gel column chromatography (hexane/ethyl acetate=9/1 to 4/1) to obtain the entitled compound (330 mg).

Aufarbeitung

  1. temperatureheated overnight
  2. temperatureunder reflux
  3. concentrationThe reaction solution was concentrated under reduced pressure, water
  4. additionwas added to the residue
  5. extractionextracted with ethyl acetate
  6. dry with materialThe organic layer was dried with anhydrous magnesium sulfate
  7. customthe solvent was evaporated off under reduced pressure
  8. customThe resulting residue was purified through silica gel column chromatography (hexane/ethyl acetate=9/1 to 4/1)

Quellen und Nachweise

ORD-Eintrag
ord-f64f79adb6b34edf968c5c9d01d79905
Quelldatensatz
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07566781B2

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