Hydrazine hydrate (1:1) → HCID 178434515, Verbindung

HRID 45514

Reaktionsgleichung

Reaktionsgleichung von HRID 45514
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9](=O)[CH3:10])=[CH:4][CH:3]=1.COC(OC)[N:15]([CH3:17])C.O.[NH2:21]N>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:9]([CH3:10])=[N:21][NH:15][CH:17]=2)=[CH:4][CH:3]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

To 4-bromophenylacetone (5.0 g, 23.5 mmol, 1.0 equiv) (Acros Organics 34216) was added N,N-dimethylformamide dimethyl acetal (11.3 ml, 84.6 mmol, 3.6 equiv) and the mixture was heated to 90° C. for 6 hours. The solvents were removed and the resulting gum was dissolved in ethanol (235 ml) with additional heating. Hydrazine hydrate (1.37 ml, 28.2 mmol, 1.2 equiv) was added and the mixture was heated to reflux for 15 hours. The solvents were removed under reduced pressure and the solid was triturated with dichloromethane to afford the title compound, 2.24 g (40%); LCMS (PS-A) Rt 2.87 min [M+H]+ 238. Further material could be isolated from the mother liquor.

Aufarbeitung

  1. customThe solvents were removed
  2. dissolutionthe resulting gum was dissolved in ethanol (235 ml) with additional heating
  3. temperaturethe mixture was heated
  4. temperatureto reflux for 15 hours
  5. customThe solvents were removed under reduced pressure
  6. customthe solid was triturated with dichloromethane

Quellen und Nachweise

ORD-Eintrag
ord-be9584ba2d8b4f1cb8d212bc767c796c
Quelldatensatz
uspto-grants-2013_09
Patentnummer
US08541461B2

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