반응 #50312

ord-14dcafb71fb949968f1b507847b0c180

반응 방정식

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

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타at 0° C.
  2. 2
    기타to remove hydrogen sulfide
  3. 3
    기타The solvent was removed by distillation

실험 절차

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)).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05426188uspto-grants-1995_06