N-Methyl-3-nitroaniline → N1-Methylbenzene-1,3-diamine

HRID 1708329Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1708329
[CH3:1][NH:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([N+:9]([O-])=O)[CH:4]=1>C(O)C.[Pd]>[CH3:1][NH:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([NH2:9])[CH:4]=1

Komponenten

4

Edukt 1

HCID 219622N-Methyl-3-nitroaniline

Produkt 1

HCID 5151957N1-Methylbenzene-1,3-diamineAusbeute 96 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23938PalladiumKatalysatorHCID 702EthanolLösungsmittel

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

8 g of the precipitate was dissolved in 20 mL of 95% ethanol, 1 g of a catalyst having 5 wt. % Pd on a carbon support was added, and hydrogenation of the N-methyl-3-nitroaniline was carried out at 50 psig (337 kPa gage) for about 10 minutes, during which time the temperature increased to about 70° C. The hydrogenated mixture was cooled to room temperature, filtered to recover the solids, which were then washed with methanol and the liquid filtrates combined. Finally, the liquids were concentrated under vacuum and distilled through a short path Kugelrohr oven at about 140° C. and 3 torr to produce a 96% yield of N-methyl m-phenylenediamine.

Aufarbeitung

  1. additionwas added
  2. temperatureThe hydrogenated mixture was cooled to room temperature
  3. filtrationfiltered
  4. customto recover the solids, which
  5. washwere then washed with methanol
  6. concentrationFinally, the liquids were concentrated under vacuum
  7. distillationdistilled through a short path Kugelrohr oven at about 140° C.

Quellen und Nachweise

ORD-Eintrag
ord-cfb6eb30a1114e468545a4101a88ba67
Quelldatensatz
uspto-grants-1994_10
Patentnummer
US05358745

Notizen zur Reaktion

Wird geladen…