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Dimethylamine → 3-Chloro-N,N-dimethylpyrazin-2-amine

HRID 1701736
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1701736
Cl[C:2]1[C:7]([Cl:8])=[N:6][CH:5]=[CH:4][N:3]=1.[CH3:9][NH:10][CH3:11]>>[Cl:8][C:7]1[C:2]([N:10]([CH3:11])[CH3:9])=[N:3][CH:4]=[CH:5][N:6]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 674DimethylamineHCID 785752,3-Dichloropyrazine

Produkt 1

HCID 204834273-Chloro-N,N-dimethylpyrazin-2-amine

Versuchsvorschrift

74 g of 2,3-dichloro-pyrazine are added dropwise over the course of 15 minutes, whilst stirring, to 350 ml of a 40% strength aqueous solution of dimethylamine. Whilst doing so, the reaction temperature is kept at 30° C. by cooling. When the exothermic reaction has subsided the mixture is stirred for a further 15 hours at room temperature. The reaction mixture is then extracted by shaking with ether. The ether extracts are washed with water until neutral, dried over sodium sulphate and evaporated in a waterpump vacuum. The residue is distilled in a waterpump vacuum. 2-Chloro-3-dimethylamino-pyrazine, boiling point 100°-102° C./10 mm Hg, is thus obtained.

Aufarbeitung

  1. customis kept at 30° C.
  2. temperatureby cooling
  3. customWhen the exothermic reaction
  • extractionThe reaction mixture is then extracted
  • stirringby shaking with ether
  • washThe ether extracts are washed with water until neutral,
  • dry with materialdried over sodium sulphate
  • customevaporated in a waterpump vacuum
  • distillationThe residue is distilled in a waterpump vacuum
  • Quellen und Nachweise

    ORD-Eintrag
    ord-c660aa2b0ef545c1924734c324297d1d
    Quelldatensatz
    uspto-grants-1980_03
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US04195090

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