Reaktion #5413

ord-d71d3da489d640ec9419ef589183bfc0

Reaktionsgleichung

Nc1cccc(C(F)(F)F)c1
3-trifluoromethylaniline
C#CCBr
propargyl bromide
C#CCNc1cccc(C(F)(F)F)c1
N-propargyl-3-trifluoromethylaniline
Ausbeute 34.8%

Reaktionsbedingungen

Temperatur
80°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Filtrationfollowed by filtration of the reaction mixture

Vorschrift

A mixture of 3-trifluoromethylaniline (30 g) ad propargyl bromide (12 g) was stirred at 80° C. for 3 hours, followed by filtration of the reaction mixture. The filtrate was subjected to column chromatography to give N-propargyl-3-trifluoromethylaniline (7 g). A solution of N-propargyl-3-trifluoromethylaniline thus obtained (5.1 g) and ethoxycarbonyl isothiocyalate (3.7 g) in tetrahydrofuran (100 ml) was stirred at room temperature for 8 hours, and the solvent was removed under reduced pressure. The concentrated residue was extracted with chloroform (200 ml), washed with water and dried over anhydrous magnesium sulfate. After removal of the solvent, the residue was subjected to column chromatography to give 5.7 g of 2 -ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-methylenethiazolidine (Compound (i)).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05244863uspto-grants-1993_09