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Imidazole → N-1H-Inden-3-ylacetamide

HRID 1582778
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1582778
[C:1]1(=[N:10]O)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH2:2]1.N1C=CN=C1.[C:17](OC(=O)C)(=[O:19])[CH3:18].C(=O)([O-])[O-].[Na+].[Na+]>C(#N)C.C([O-])(=O)C.C([O-])(=O)C.C([O-])(=O)C.[Ti+3]>[C:17]([NH:10][C:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH:2]=1)(=[O:19])[CH3:18]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 795ImidazoleHCID 7918Acetic Anhydride2×HCID 10340Sodium CarbonateHCID 3023232,3-Dihydro-1H-inden-1-one oxime

Produkt 1

HCID 10130185N-1H-Inden-3-ylacetamideAusbeute 61,3 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 14117218
HCID 14117218, Verbindung
Katalysator
HCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

1-Indanone oxime (2.33 g, 0.016 moles) and imidazole (78 mg) in acetonitrile (45 ml) cooled in ice, were treated with acetic anhydride (11 ml, 0.12 moles) and the mixture thus stirred for one hour. Titanium triacetate (17 g) was added, followed by more acetic anhydride (11 ml, 0.12 moles). The mixture was brought to reflux under nitrogen. After 2 hours the mixture was allowed to cool, poured into 1M sodium carbonate (250 ml) and stirred for 15 minutes. Three-fold extraction with ethyl acetate, drying (MgSO4) and evaporation left a brown oil which was reevaporated with toluene. The brown residue was subjected to flash chromatography on silica gel with ethyl acetate/hexane 1:2 v/v. The major component was obtained as a white solid (1.7 g) from the appropriate fractions and was recrystallized from ethyl acetate/hexane to give the title compound, mp 137-138° C. (1.45 g, 52.9%).

Aufarbeitung

  1. temperatureto reflux under nitrogen
  2. waitAfter 2 hours the mixture was allowed
  3. temperatureto cool
  4. stirringstirred for 15 minutes
  5. extractionThree-fold extraction with ethyl acetate
  6. customdrying
  7. custom(MgSO4) and evaporation
  8. waitleft a brown oil which
  9. customwas reevaporated with toluene

Quellen und Nachweise

ORD-Eintrag
ord-d94c586946924f86bae69c005a79c13c
Quelldatensatz
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06737547B1

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