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Ethylenediamine → HCID 21463158, Verbindung

HRID 1940979
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1940979
O=[C:2]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[C:5]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[C:4]([C:18]([OH:20])=O)[O:3]1.[CH2:21]([NH2:24])[CH2:22][NH2:23]>>[O:20]=[C:18]1[C:4]2[N:24]([C:2](=[O:3])[C:7]3[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=3[C:5]=2[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH2:21][CH2:22][NH:23]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 3301EthylenediamineHCID 42017421-oxo-4-phenyl-1H-isochromene-3-carboxylic acid

Produkt 1

HCID 21463158HCID 21463158, Verbindung

Versuchsvorschrift

A mixture of 1-oxo-4-phenyl-1H-2-benzopyran-3-carboxylic acid (500 mg) and ethylenediamine (15 ml) was stirred at room temperature overnight. After evaporation of the solvent, concentrated hydrochloric acid (10 ml) and acetic acid (10 ml) were added to the residue. The mixture was heated under reflux for 48 hours. To the mixture was added water, and extracted with ethyl acetate. The extract was washed successively with water, aqueous sodium hydrogen carbonate and water, dried, and evaporated to yield the title compound as colorless crystals (115 mg).

Aufarbeitung

  1. customAfter evaporation of the solvent, concentrated hydrochloric acid (10 ml) and acetic acid (10 ml)
  2. additionwere added to the residue
  • temperatureThe mixture was heated
  • temperatureunder reflux for 48 hours
  • additionTo the mixture was added water
  • extractionextracted with ethyl acetate
  • washThe extract was washed successively with water, aqueous sodium hydrogen carbonate and water
  • customdried
  • customevaporated
  • Quellen und Nachweise

    ORD-Eintrag
    ord-ea8907fe1ee34b42b5b4d859cd674457
    Quelldatensatz
    uspto-grants-1997_12
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US05700810

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