تفاعل #50312

ord-14dcafb71fb949968f1b507847b0c180

معادلة التفاعل

S
Hydrogen sulfide
C#CCN(C#N)c1cccc(C(F)(F)F)c1
N-cyano-N-propargyl-3-trifluoromethylaniline
CCN(CC)CC
triethylamine
C=C1CN(c2cccc(C(F)(F)F)c2)C(=N)S1
2-imino-3-(3-trifluoromethylphenyl)-5-methylenethiazolidine

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىat 0° C.
  2. 2
    أخرىto remove hydrogen sulfide
  3. 3
    أخرىThe solvent was removed by distillation

الإجراء التجريبي

To a solution of N-cyano-3-trifluoromethylaniline (5.0 g) in acetone (100 ml) , potassium carbonate (7.4 g) and propargyl bromide (3.5 g) were added, and the resultant mixture was stirred at room temperature for 10 hours, followed by filtration of the reaction mixture. The solvent was removed from the filtrate by distillation under reduced pressure, and the residue was subjected to column chromatography to give N-cyano-N-propargyl-3-trifluoromethylaniline (3.8 g). The thus obtained N-cyano-N-propargyl-3-trifluoromethylaniline (1 g) and a catalytic amount of triethylamine were dissolved in methanol (30 ml), and the resultant mixture was cooled to 0° C. Hydrogen sulfide was gradually introduced into the mixture for 20 minutes while keeping the temperature at 0° C., followed by introduction of nitrogen gas to remove hydrogen sulfide. The solvent was removed by distillation, and the residue was subjected to column chromatography to give 0.2 g of 2-imino-3-(3-trifluoromethylphenyl)-5-methylenethiazolidine (Compound (ix)).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05426188uspto-grants-1995_06