Hydrazine hydrate (1:1) → HCID 10199104, Verbindung

HRID 395921Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 395921
O.[NH2:2][NH2:3].[Cl:4][C:5]1[CH:10]=[CH:9][C:8]([C:11](=O)[C:12]#[C:13][C:14]2[S:15][CH:16]=[CH:17][CH:18]=2)=[CH:7][CH:6]=1>C(O)C.C1(C)C=CC(S([O-])(=O)=O)=CC=1.[NH+]1C=CC=CC=1>[Cl:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[CH:12]=[C:13]([C:14]3[S:15][CH:16]=[CH:17][CH:18]=3)[NH:3][N:2]=2)=[CH:7][CH:6]=1

Komponenten

5

Edukt 2

HCID 24654Hydrazine hydrate (1:1)HCID 13360982HCID 13360982, Verbindung

Produkt 1

HCID 10199104HCID 10199104, VerbindungAusbeute 80 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 466102Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)KatalysatorHCID 702EthanolLösungsmittel

Versuchsvorschrift

Hydrazine hydrate (228 mg, 4.6 mM) and pyridinium p-toluenesulfonate (50 mg) were added to a solution of 1-(4-chlorophenyl)-3-(2-thienyl)-2-propyn-1-one (750 mg, 3.0 mM) in ethanol (30 ml), and this mixture was heated under reflux for 2 hours. After the mixture was allowed to cool to room temperature, the solvent was distilled off under reduced pressure, and the resulting residue was dissolved in ethyl acetate (50 ml). This solution was washed with a saturated aqueous solution of sodium hydrogen carbonate and a saturated aqueous solution of sodium chloride, and dried over magnesium sulfate. Thereafter, the solvent was distilled off under reduced pressure to obtain 634 mg of 3-(4-chlorophenyl)-5-(2-thienyl)-1H-pyrazole, m.p. 217° C., in an 80% yield.

Aufarbeitung

  1. temperaturethis mixture was heated
  2. temperatureunder reflux for 2 hours
  3. distillationthe solvent was distilled off under reduced pressure
  4. dissolutionthe resulting residue was dissolved in ethyl acetate (50 ml)
  5. washThis solution was washed with a saturated aqueous solution of sodium hydrogen carbonate
  6. dry with materiala saturated aqueous solution of sodium chloride, and dried over magnesium sulfate
  7. distillationThereafter, the solvent was distilled off under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-16672854e8c643fb87fb9437dbc1d43f
Quelldatensatz
uspto-grants-2003_08
Patentnummer
US06605730B2

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