Reaktion #417963

ord-4b5a523603fd4ce2a4d381c05c57e5fa

Reaktionsgleichung

N
ammonia
[Na]
sodium
COc1cc(Cl)ccc1Cl
2,5-dichloroanisole
N
ammonia
[Na]
sodium
COc1cc(N)ccc1Cl
4-chloro-3-methoxyaniline
Ausbeute 99.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
-78°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigecondensed at −78° C
  2. 2
    Temperaturthe reaction warmed to −45° C. for 2 hrs
  3. 3
    Sonstigeto evaporate
  4. 4
    workup.ADDITIONThe crude pot was then diluted in chloroform
  5. 5
    workup.ADDITION100 g of NH4Cl was added slowly
  6. 6
    SonstigeThe combines were taken up in a separatory funnel
  7. 7
    Waschenwashed with water (3×)
  8. 8
    TrocknenThe organic layer was dried over sodium sulfate
  9. 9
    Einengenconcentrated in vacuo
  10. 10
    SonstigeThe resulting solid can be used without further purification

Vorschrift

900 mL of ammonia was condensed at −78° C. 1 g of thinly shaven strips of sodium was added followed by 1.0 g of iron (III) nitrate nonahydrate. Upon disappearance of the deep blue color 25 g of thinly shaven strips of sodium was added. After 30 mins of stirring at −78° C., 50 g of 2,5-dichloroanisole was added as a solution in hexane (70 mL) dropwise and the reaction warmed to −45° C. for 2 hrs. Upon completion the ammonia was allowed to evaporate. The crude pot was then diluted in chloroform and 100 g of NH4Cl was added slowly. The combines were taken up in a separatory funnel and washed with water (3×) followed by brine (1×). The organic layer was dried over sodium sulfate and concentrated in vacuo. The resulting solid can be used without further purification. Yield: 99%.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08877752B2uspto-grants-2014_11