Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5317Erstellt: 23. Oktober 2026

3-(Trifluoromethyl)aniline → Benzenamine, N-2-propyn-1-yl-3-(trifluoromethyl)-

https://huagongshe.com/de/reaction/5317

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-(Trifluoromethyl)anilineHCID 7375—
EduktPropargyl bromideHCID 7842—
ProduktBenzenamine, N-2-propyn-1-yl-3-(trifluoromethyl)-HCID 1048821334,8%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

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)).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05244863
Quelldatensatzuspto-grants-1993_09
ORD IDord-d71d3da489d640ec9419ef589183bfc0
Quellennotizuspto-grants-1993_09