반응 #214784

ord-6f00d3033d3645a696bfbbe800260853

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도warmed for 5 minutes on the steam cone until
  2. 2
    workup.DISSOLUTIONall is dissolved
  3. 3
    기타the precipitate formed
  4. 4
    기타is collected
  5. 5
    workup.ADDITIONthe solution added to the mixture of 3 ml of 5 N hydrochloric acid and 250 ml of water
  6. 6
    기타The crude product formed
  7. 7
    기타is collected
  8. 8
    세척washed with water
  9. 9
    workup.DISSOLUTIONdissolved in 5% aqueous sodium hydroxide
  10. 10
    여과filtered
  11. 11
    기타The precipitate is collected
  12. 12
    세척washed with water
  13. 13
    기타air-dried
  14. 14
    기타recrystallized from ethanol

실험 절차

The suspension of 1.0 g of 1,2,5-trimethyl-β-oxo-3-pyrrolpropionitrile, 40 ml of toluene and 0.7 g of triethylamine is treated with 0.75 g of phenylisocyanate and warmed for 5 minutes on the steam cone until all is dissolved. After standing overnight, the precipitate formed is collected, taken up in methanol, and the solution added to the mixture of 3 ml of 5 N hydrochloric acid and 250 ml of water. The crude product formed is collected, washed with water, dissolved in 5% aqueous sodium hydroxide, filtered, and the alkaline filtrate acidified with 5 N hydrochloric acid. The precipitate is collected, washed with water, air-dried and recrystallized from ethanol, to yield the 1,2,5-trimethyl-β-oxo-α-phenylcarbamoyl-3-pyrrolpropionitrile melting at 158°-160°.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04256759uspto-grants-1981_03