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M-Cresol → 3-(3-Methylphenoxy)benzaldehyde

HRID 2422252
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2422252
Br[C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6].[CH:10]1[C:15]([OH:16])=[CH:14][CH:13]=[CH:12][C:11]=1[CH3:17].C(=O)([O-])[O-].[K+].[K+].N1C2C(=CC=CC=2)C=CC=1>[Cu]=O.N1C=CC=CC=1>[CH3:17][C:11]1[CH:10]=[C:15]([CH:14]=[CH:13][CH:12]=1)[O:16][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 342M-CresolHCID 7047QuinolineHCID 11430Potassium CarbonateHCID 765833-Bromobenzaldehyde

Produkt 1

HCID 230829033-(3-Methylphenoxy)benzaldehydeAusbeute 72,1 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 14829
Copper oxide
Katalysator
HCID 1049PyridineLösungsmittel

Reaktionsbedingungen

Temperatur
170 °C

Versuchsvorschrift

A mixture of 3-bromobenzaldehyde (7.01 g, 37.9 mmol), m-cresol (4.51 g, 41.7 mmol), copper oxide (II) (4.53 g, 56.9 mmol), potassium carbonate (7.86 g, 56.9 mmol), pyridine (50 mL) and quinoline (25 mL) was stirred under a nitrogen atmosphere at 170° C. for 24 hrs. The reaction mixture was cooled and pyridine was evaporated under reduced pressure. Ethyl acetate was added to the residue, the insoluble material was filtered off, and the filtrate was washed with 1 M hydrochloric acid and saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (hexane-10% ethyl acetate/hexane) to give the title compound (5.80 g, 72%) as a pale-brown oil.

Aufarbeitung

  1. temperatureThe reaction mixture was cooled
  2. custompyridine was evaporated under reduced pressure
  3. additionEthyl acetate was added to the residue
  4. filtrationthe insoluble material was filtered off
  5. washthe filtrate was washed with 1 M hydrochloric acid and saturated brine
  6. dry with materialdried over anhydrous sodium sulfate
  7. customThe solvent was evaporated under reduced pressure
  8. customthe residue was purified by silica gel column chromatography (hexane-10% ethyl acetate/hexane)

Quellen und Nachweise

ORD-Eintrag
ord-83e5591d14fe4cd6aa276420a9bd8bc1
Quelldatensatz
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07960369B2

Notizen zur Reaktion

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