반응 #311761

ord-037e80eb8c024dc6b5576410f1326880

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타were passed in at -10° C
  2. 2
    온도whilst cooling
  3. 3
    workup.ADDITIONwere added
  4. 4
    workup.STIRRINGThis mixture was first stirred for 2 hours at room temperature
  5. 5
    온도was then heated
  6. 6
    기타(5 to 6 hours)
  7. 7
    온도After cooling
  8. 8
    여과the mixture was filtered
  9. 9
    세척the residue was washed with acetonitrile
  10. 10
    농축the entire filtrate was concentrated by evaporation in vacuo
  11. 11
    온도cooled to -10° to -15° C
  12. 12
    기타The colorless crystals which had precipitated
  13. 13
    여과were filtered off
  14. 14
    기타dried

실험 절차

17 g (0.2 mole) of 2-cyanoethylhydrazine were dissolved in 100 ml of acetonitrile and 7.3 g of hydrogen chloride gas were passed in at -10° C. Thereafter, 32 g of N-chlorocarbonylisocyanide dichloride were added dropwise at 0° C., whilst cooling and stirring well, and after completion of this addition, 30 g of potassium carbonate were added. This mixture was first stirred for 2 hours at room temperature and was then heated under reflux until no further evolution of hydrogen chloride was detectable (5 to 6 hours). After cooling, the mixture was filtered, the residue was washed with acetonitrile and the entire filtrate was concentrated by evaporation in vacuo. The oil which remained was taken up in a little ethanol and cooled to -10° to -15° C. The colorless crystals which had precipitated were filtered off and dried. 20 g of 1-(2-cyanoethyl)-5-chloro-3-hydroxy-1,2,4-triazole of melting point 149°-150° C. were obtained. ##STR23##

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04233293uspto-grants-1980_11