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Toluene → 5-(4-Ethoxyphenyl)-2-fluorobenzaldehyde

HRID 413586
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 413586
Br[C:2]1[CH:3]=[CH:4][C:5]([F:10])=[C:6]([CH:9]=1)[CH:7]=[O:8].[CH2:11]([O:13][C:14]1[CH:19]=[CH:18][C:17](OB(O)O)=[CH:16][CH:15]=1)[CH3:12].C(=O)([O-])[O-].[Na+].[Na+].C1(C)C=CC=CC=1>COCCOC>[CH2:11]([O:13][C:14]1[CH:19]=[CH:18][C:17]([C:2]2[CH:3]=[CH:4][C:5]([F:10])=[C:6]([CH:9]=2)[CH:7]=[O:8])=[CH:16][CH:15]=1)[CH3:12]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 1140TolueneHCID 10340Sodium CarbonateHCID 7363275-Bromo-2-fluorobenzaldehydeHCID 185333934-Ethoxyphenylboric acid

Produkt 1

HCID 185333825-(4-Ethoxyphenyl)-2-fluorobenzaldehydeAusbeute 76 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8071
1,2-Dimethoxyethane
Lösungsmittel
3×

Versuchsvorschrift

Under an argon atmosphere, tetrakistriphenylphosphine palladium (69 mg) was added to 5 ml of 1,2-dimethoxyethane. A mixture resulting from dissolving 5-bromo-2-fluorobenzaldehyde (406 mg) in 5 ml of 1,2-dimethoxyethane was added. A mixture resulting from dissolving 4-ethoxyphenylboric acid (398 mg) in 1.5 ml of 1,2-dimethoxyethane was added. Two milliliter of 2M sodium carbonate solution was added. Stirring was conducted for one hour and ten minutes under reflux. After cooling to room temperature, 20 ml of toluene was added and was washed with 10 ml of water twice, 10 ml of a 2N sodium hydroxide solution twice and 10 ml of water twice. After drying with anhydrous sodium sulfate, the mixture was concentrated. The concentrated matter was purified by silica gel chromatography (hexane/ethyl acetate=4/1). The resulting effective fractions were concentrated to yield 5-(4-ethoxyphenyl)-2-fluorobenzaldehyde (369 mg, Yield 76%).

Aufarbeitung

  1. customA mixture resulting
  2. additionwas added
  3. customA mixture resulting
  4. additionwas added
  5. temperatureunder reflux
  6. washwas washed with 10 ml of water twice
  7. dry with materialAfter drying with anhydrous sodium sulfate
  8. concentrationthe mixture was concentrated
  9. customThe concentrated matter was purified by silica gel chromatography (hexane/ethyl acetate=4/1)
  10. concentrationThe resulting effective fractions were concentrated

Quellen und Nachweise

ORD-Eintrag
ord-f576b0cafd1446609f005be81cd75e7f
Quelldatensatz
uspto-grants-2003_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06566535B1

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