4-Chloropyridine → 4-Hydrazinylpyridine hydrochloride

HRID 497996

Reaktionsgleichung

Reaktionsgleichung von HRID 497996
[Cl:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1.O.[NH2:9][NH2:10]>C(O)CC>[ClH:1].[NH:9]([C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1)[NH2:10]

Komponenten

4

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

The title compound was prepared according to the method described in J. Chem. Soc., p. 3830 (1959). A solution of 4-chloropyridine (16.5 g, 145 mmol) and hydrazine monohydrate (7.76 mL, 160 mmol) in 1-propanol (50 mL) was heated under reflux for 18 hours. The solution was cooled to 0° C., and the resulting crystals were collected by filtration. The crystals were washed with cold 1-propanol and air dried to give the title compound (15.2 g, 72% yield). The compound was used in the following process without further purification.

Aufarbeitung

  1. customThe title compound was prepared
  2. temperatureunder reflux for 18 hours
  3. filtrationthe resulting crystals were collected by filtration
  4. washThe crystals were washed with cold 1-propanol and air
  5. customdried

Quellen und Nachweise

ORD-Eintrag
ord-b6a17618da274f71b76f9270d8a1ace7
Quelldatensatz
uspto-grants-2005_09
Patentnummer
US06949648B2

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