Reaktion #87860

ord-0b8cff70b7e74cb5865e34e425b77082

Reaktionsgleichung

[Na+].[Na+].[S-2]
sodium sulphide
[S]
sulphur
CC(C)c1ccc([N+](=O)[O-])cc1Br
2-bromo-1-isopropyl-4-nitrobenzene
CC(C)c1ccc([N+](=O)[O-])cc1Br
2-Bromo-1-isopropyl-4-nitrobenzene
CC(C)c1ccc(N)cc1Br
3-Bromo-4-isopropylaniline
Ausbeute 103.2%

Lösungsmittel

Reaktionsbedingungen

Temperatur
75°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGAfter stirring for another 5 hours
  2. 2
    workup.DISTILLATIONFor the work-up, the isopropanol was firstly distilled off
  3. 3
    Extraktionthe remaining mixture was extracted with toluene/chlorobenzene
  4. 4
    workup.DISTILLATIONThe combined organic phases were distilled under reduced pressure

Vorschrift

A solution of sodium sulphide (31.2 g, 0.24 mol) and sulphur (7.7 g, 0.24 mol) was stirred at 80° C. for 15 minutes. Isopropanol (160 g) was subsequently added and the mixture was stirred at 75° C. for a further 15 minutes and 2-bromo-1-isopropyl-4-nitrobenzene (XI) (50 g, 0.19 mol) was finally added dropwise over a period of 30 minutes. After stirring for another 5 hours, the reaction was complete. For the work-up, the isopropanol was firstly distilled off and the remaining mixture was extracted with toluene/chlorobenzene. The combined organic phases were distilled under reduced pressure. 3-Bromo-4-isopropylaniline (42 g, 91 GC-% by area, 93% of theory) was obtained as a red oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09440908B2uspto-grants-2016_09