1,3,5-Trichlorobenzene → 3,5-Dichlorophenylhydrazine

HRID 1635692

Reaktionsgleichung

Reaktionsgleichung von HRID 1635692
[Cl:1][C:2]1[CH:7]=[C:6](Cl)[CH:5]=[C:4]([Cl:9])[CH:3]=1.O.[NH2:11][NH2:12]>N1C=CC=CC=1>[Cl:1][C:2]1[CH:7]=[C:6]([NH:11][NH2:12])[CH:5]=[C:4]([Cl:9])[CH:3]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
180 °C

Versuchsvorschrift

A mixture of 1,3,5-trichlorobenzene (2.53 g), hydrazine hydrate (3.48 g, 5 molar equivalents) and pyridine (12 ml) was heated in an autoclave (purged with argon) for 6 hours at 180° C. The mixture was cooled, the excess hydrazine decanted and the organic phase evaporated in vacuo to give the title compound in 60% yield. It was shown that 65% of the starting material had been consumed, thus indicating that the reaction had occurred with high selectivity.

Aufarbeitung

  1. temperatureThe mixture was cooled
  2. customthe excess hydrazine decanted
  3. customthe organic phase evaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-3e6a2dccd2424f91bb0356d383f5ee0e
Quelldatensatz
uspto-grants-2003_01
Patentnummer
US06509503B1

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