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Dimethylformamide → 2-Isopropyl-6-methylbenzaldehyde

HRID 427510
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 427510
Br[C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][C:3]=1[CH:9]([CH3:11])[CH3:10].[Mg].CN(C)[CH:15]=[O:16]>C(OCC)C>[CH:9]([C:3]1[CH:4]=[CH:5][CH:6]=[C:7]([CH3:8])[C:2]=1[CH:15]=[O:16])([CH3:11])[CH3:10]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 6228DimethylformamideHCID 5462224MagnesiumHCID 145345702-Bromo-1-isopropyl-3-methylbenzene

Produkt 1

HCID 124670472-Isopropyl-6-methylbenzaldehydeAusbeute 33 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

To a solution of 1-bromo-2-isopropyl-6-methylbenzene (6.9 g, 32.4 mmol) in diethyl ether (50 ml) was added magnesium turnings (0.9 g, 37 mmol) and the mixture was refluxed in nitrogen atmosphere until the reaction was started and was then stirred overnight at room temperature. Dimethylformamide (4 ml) was added dropwise during 10 min. and the mixture was stirred for 30 min. Saturated ammmoniumchloride solution (30 ml) was added and the mixture was stirred for 1 h. The organic layer was separated, filtrated and evaporated under reduced pressure. Purification by column chromatography on silica gel using hexane:methylene chloride (3:2) as eluent gave 1.75 g (33%) of the title compound .

Aufarbeitung

  1. temperaturethe mixture was refluxed in nitrogen atmosphere until the reaction
  2. stirringthe mixture was stirred for 30 min
  3. stirringthe mixture was stirred for 1 h
  4. customThe organic layer was separated
  5. filtrationfiltrated
  6. customevaporated under reduced pressure
  7. customPurification by column chromatography on silica gel

Quellen und Nachweise

ORD-Eintrag
ord-bb5ea198fbde4afeb2dd934f21b8792d
Quelldatensatz
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06313137B1

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