O-Xylene → 2-Amino-4'-chlorobiphenyl

HRID 534710Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 534710
C1(C)C(C)=CC=CC=1.[Cl:9][C:10]1[CH:15]=[CH:14][C:13]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[N+:22]([O-])=O)=[CH:12][CH:11]=1>[Pt].CC(C)=O>[Cl:9][C:10]1[CH:11]=[CH:12][C:13]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[NH2:22])=[CH:14][CH:15]=1

Komponenten

5

Edukt 2

HCID 7237O-XyleneHCID 2355494'-Chloro-2-nitro-1,1'-biphenyl

Produkt 1

HCID 2622612-Amino-4'-chlorobiphenyl

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23939PlatinumKatalysatorHCID 180AcetoneLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

In a 20 ml autoclave were placed 1 g of xylene, 6 mg of a Pt/C catalyst (containing 1% by weight of Pt with respect to the weight of carbon) and 0.25 g (1 mmol) of 4′-chloro-2-nitrobiphenyl obtained in example 1.4. The mixture was stirred under hydrogen pressure (7-8 bar) at 100° C. until the starting material had disappeared (monitoring via HPLC). After completion of the reaction the mixture was cooled to ambient temperature and diluted with 15 ml of acetone. The catalyst was filtered off and the filtrate was evaporated in vacuo yielding 0.2 g (91% of theory) of the title compound in a purity of 93% (HPLC % by weight).

Aufarbeitung

  1. customAfter completion of the reaction the mixture
  2. temperaturewas cooled to ambient temperature
  3. filtrationThe catalyst was filtered off
  4. customthe filtrate was evaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-7edf882425b346a5b8725fcdced879a2
Quelldatensatz
uspto-grants-2014_10
Patentnummer
US08853455B2

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