StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Ethanol → 4-Isobutylbenzaldehyde oxime

HRID 2247678
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2247678
[CH2:1]([C:5]1[CH:12]=[CH:11][C:8]([CH:9]=O)=[CH:7][CH:6]=1)[CH:2]([CH3:4])[CH3:3].C(O)C.N1C=CC=CC=1.Cl.[NH2:23][OH:24]>CCOCC.O>[CH2:1]([C:5]1[CH:12]=[CH:11][C:8]([CH:9]=[N:23][OH:24])=[CH:7][CH:6]=1)[CH:2]([CH3:4])[CH3:3]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 702EthanolHCID 1049PyridineHCID 443297Hydroxyamine hydrochlorideHCID 577537Benzaldehyde, 4-(2-methylpropyl)-

Produkt 1

HCID 802569644-Isobutylbenzaldehyde oximeAusbeute 84 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962Water
Lösungsmittel
HCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

To a solution of 4-isobutylbenzaldehyde (5.0 g, 31 mmol) in a mixed solvent of ethanol (25 ml) and pyridine (25 ml) was added hydroxylamine hydrochloride (2.4 g, 34 mmol) with stirring, and the resulting mixture was stirred at room temperature for 18 hours. After evaporating the reaction mixture in vacuo, the residue thus obtained was diluted with ether, poured into water (150 ml) and extracted with ether. The extract was washed successively with 1N hydrochloric acid and a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. After filtration, the filtrate was evaporated in vacuo, and the crude product of the title compound thus obtained was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (1:19 to 1:9) as the eluent to afford the title compound (4.6 g) in a yield of 84% as a colourless oily product.

Aufarbeitung

  1. stirringthe resulting mixture was stirred at room temperature for 18 hours
  2. customAfter evaporating the reaction mixture in vacuo
  3. customthe residue thus obtained
  4. extractionextracted with ether
  5. washThe extract was washed successively with 1N hydrochloric acid
  6. dry with materiala saturated aqueous solution of sodium chloride and dried over magnesium sulfate
  7. filtrationAfter filtration
  8. customthe filtrate was evaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-d46253ce467a462ebd250c6065799f66
Quelldatensatz
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07687491B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion