تفاعل #6036

ord-97a71ab8b30846a79c74a25e489cdea9

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added to the mixture
  2. 2
    workup.WAITto stand at room temperature overnight
  3. 3
    أخرىThe solvent was removed from the reaction mixture under reduced pressure and water
  4. 4
    workup.ADDITIONwas added to the residue
  5. 5
    استخلاصThe mixture was extracted with 50 ml of ethyl acetate
  6. 6
    أخرىdried
  7. 7
    أخرىcondensed under reduced pressure
  8. 8
    أخرىpurified by silica gel chromatography
  9. 9
    أخرىrecrystallized from hexane

الإجراء التجريبي

To a 10 ml tetrahydrofuran solution containing 1.00 g (6 mmole) of 4-chlorophenylmethylbenzylcyanide was added a 3.2 ml tetrahydrofuran solution containing 2 M of lithium diisopropylamide at -60° C. After stirring for 30 minutes under the same conditions, a 5 ml tetrahydrofuran solution containing 0.44 g (6 mmol) of methyl isothiocyanate was added to the mixture and the mixture was allowed to stand at room temperature overnight. The solvent was removed from the reaction mixture under reduced pressure and water was added to the residue. The mixture was extracted with 50 ml of ethyl acetate, dried and condensed under reduced pressure, and then purified by silica gel chromatography and recrystallized from hexane to obtain 0.45 g (yield: 31.4 %) of N-methyl-2-(4-chlorophenyl)-2-cyano-thiopropionamide.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05246958uspto-grants-1993_09