Acetone → HCID 178524616, Verbindung

HRID 1700783

Reaktionsgleichung

Reaktionsgleichung von HRID 1700783
[OH:1][C:2]1[CH:10]=[C:9]([C:11]([OH:13])=[O:12])[C:8]([OH:14])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].C(=O)([O-])[O-].[Cs+:19].[Cs+].CC(C)=O>O>[OH:1][C:2]1[CH:10]=[C:9]([C:11]([O-:13])=[O:12])[C:8]([OH:14])=[CH:7][C:3]=1[C:4]([O-:6])=[O:5].[Cs+:19].[Cs+:19]

Komponenten

5

Edukt 3

HCID 180AcetoneHCID 10796Cesium carbonateHCID 691312,5-Dihydroxyterephthalic acid

Produkt 1

HCID 178524616HCID 178524616, VerbindungAusbeute 200 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

0.5 mol of 2,5-dihydroxyterephthalic acid and 0.5 mol of cesium carbonate were added to 200 ml of acetone and 200 ml of water and dissolved therein by stirring. After completely dissolving, the resultant solution was concentrated to dryness to give 0.5 mol of cesium 2,5-dihydroxyterephthalate. 46.2 g (0.1 mol) of cesium 2,5-dihydroxyterephthalate, 38.62 g (0.2 mol) of bromooctane and 400 ml of DMF were introduced into a reactor and reacted under a nitrogen gas stream at 100° C. for 3 hours. The reaction solution was concentrated, washed with water and dried to give 40.1 g (0.95 mol) of 2,5-dihydroxybenzene-1,6-dicarboxylic octane.

Aufarbeitung

  1. dissolutiondissolved
  2. dissolutionAfter completely dissolving
  3. concentrationthe resultant solution was concentrated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-3eb14a43b8784f7e81ce057f4737fc33
Quelldatensatz
uspto-grants-2002_02
Patentnummer
US06350845B1

Verknüpfte Notizen

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