Hydrochloric Acid → HCID 53690663, Verbindung

HRID 544164Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 544164
[CH3:1][C:2]1[O:3][C:4]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[CH:5][C:6](=[O:8])[CH:7]=1.[C:15]([C:18]1[CH:25]=[CH:24][C:21]([CH:22]=O)=[CH:20][CH:19]=1)([OH:17])=[O:16].[O-]CC.[Na+].[Na].Cl>C(O)C>[O:8]=[C:6]1[CH:5]=[C:4]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[O:3][C:2]([CH:1]=[CH:22][C:21]2[CH:24]=[CH:25][C:18]([C:15]([OH:17])=[O:16])=[CH:19][CH:20]=2)=[CH:7]1

Komponenten

7

Versuchsvorschrift

2-Methyl-6-phenyl-4H-pyran-4-one (3.7 g) and 4-carboxybenzaldehyde (3.0 g) were added to a stirred solution of sodium ethoxide prepared by dissolving sodium (1.0 g) in ethanol (75 ml) and the mixture was heated under reflux for an hour, cooled and acidified with 2M hydrochloric acid (25 ml). The resulting solid was recrystallised from acetic acid and then from dimethylformamide-water to give the pale yellow title product (mp>300° C.).

Aufarbeitung

  1. customprepared
  2. temperaturethe mixture was heated
  3. temperatureunder reflux for an hour
  4. temperaturecooled
  5. customThe resulting solid was recrystallised from acetic acid

Quellen und Nachweise

ORD-Eintrag
ord-a50fb457204647888acf6e4823bced91
Quelldatensatz
uspto-grants-1984_05
Patentnummer
US04448787

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