Reaktion #55471

ord-524568bf38ce4974b03d5afbfa84b9a8

Reaktionsgleichung

Cl
hydrogen chloride
CNc1c(Cl)cccc1Cl
N-methyl-2,6-dichloroaniline
Cl
HCl
Cc1cccc(O)c1
m-cresol
[Na+].[OH-]
sodium hydroxide
N#CN
cyanamide
CN(C(=N)N)c1c(Cl)cccc1Cl.Cl
1-(2,6-dichlorophenyl)-1-methylguanidine hydrochloride

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturheated on a steam bath
  2. 2
    Temperaturthen heated for 2 hours on a steam bath
  3. 3
    TemperaturThe reaction mixture is then cooled
  4. 4
    Temperaturcooled
  5. 5
    Extraktionextracted with 2 liters of ether
  6. 6
    WaschenThe ether layer is washed with 2×1 liter of water
  7. 7
    Trocknendried over sodium sulfate
  8. 8
    Sonstigeevaporated
  9. 9
    SonstigeThe residue is triturated with hexane
  10. 10
    Filtrationthe precipitate is filtered off
  11. 11
    Waschenwashed with ether
  12. 12
    Sonstigedried

Vorschrift

To 55.4 g (0.315 mole) of N-methyl-2,6-dichloroaniline is added 0.4 moles of ethereal HCl and 200 ml of m-cresol. The mixture is then stirred and heated on a steam bath to drive off the ether and excess hydrogen chloride. To the resultant mixture is then added 13.3 g (0.315 mole) of cyanamide then heated for 2 hours on a steam bath. The reaction mixture is then cooled, added to 150 ml of conc. sodium hydroxide solution, cooled and extracted with 2 liters of ether. The ether layer is washed with 2×1 liter of water, dried over sodium sulfate, charcoaled and evaporated. The residue is triturated with hexane and the precipitate is filtered off and washed with ether and dried to obtain 1-(2,6-dichlorophenyl)-1-methylguanidine hydrochloride.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04220658uspto-grants-1980_09