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Acetic Acid → N-(3-formyl-2-methylphenyl)acetamide

HRID 2286456
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2286456
[CH3:1][C:2]1[C:9]([NH2:10])=[CH:8][CH:7]=[CH:6][C:3]=1[C:4]#N.[C:11](OC(=O)C)(=[O:13])[CH3:12].C(O)(=[O:20])C>>[CH3:1][C:2]1[C:9]([NH:10][C:11](=[O:13])[CH3:12])=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=[O:20]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 176Acetic AcidHCID 7918Acetic AnhydrideHCID 2548423-Amino-2-methylbenzonitrile

Produkt 1

HCID 20462526N-(3-formyl-2-methylphenyl)acetamide

Versuchsvorschrift

39g (0.3 mole) of 2-methyl-3-amino-benzonitrile were dissolved in 75 ml of acetic acid, 30 ml (0.3 mole) of acetic anhydride were added, the mixture was heated with reflux for 5 minutes, and cooled. The solid obtained was filtered off and the evaporation of the solent furnished an additional quantity of solid which was added to the preceding one. After recrystallisation of the whole from toluene, 44 g (95%) of colorless flakes were obtained, with a melting point of 160° C. l

Aufarbeitung

  1. temperaturethe mixture was heated
Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion
  • temperaturewith reflux for 5 minutes
  • temperaturecooled
  • customThe solid obtained
  • filtrationwas filtered off
  • customthe evaporation of the
  • customsolent furnished an additional quantity of solid which
  • additionwas added to the preceding one
  • customAfter recrystallisation of the whole from toluene, 44 g (95%) of colorless flakes
  • customwere obtained, with a melting point of 160° C. l
  • Quellen und Nachweise

    ORD-Eintrag
    ord-4e54882d31324ec0ac58cc74ee3f731a
    Quelldatensatz
    uspto-grants-1981_05
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US04266060

    Notizen zur Reaktion

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