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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 375392Erstellt: 26. Oktober 2026

Piperazine → 2-Difluoroacetylimino-3(3-trifluoromethylphenyl)-5-methylthiazoline

https://huagongshe.com/reaction/375392

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPiperazineHCID 4837—
EduktDiglymeHCID 8150—
EduktTetrafluoroethyleneHCID 8301—
EduktTriethylamineHCID 8471—
Edukt2-Imino-3-(3-trifluoromethyl-phenyl)-5-methylthiazoline hydrochlorideHCID 21480071—
Produkt2-Difluoroacetylimino-3(3-trifluoromethylphenyl)-5-methylthiazolineHCID 1108898360%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

A solution of 2-imino-3-(3-trifluoromethylphenyl)-5-methylthiazoline hydrochloride salt (1.47 g, 5.0 mmol), piperazine (0.64 g, 7.5 mmol) and triethylamine (1.52 g, 15.0 mmol) in diglyme (10 ml) charged in a reaction flask was reacted with tetrafluoroethylene, which was made to flow intothe flask (ca. 0.7 liter/hr), with vigorous stirring at 70° C. for 24 hours. After cooling to an ambient temperature, the reaction mixture was poured into ice-water, and extracted with diethyl ether. The diethyl ether layer was washed with water and then brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was subjected to silica gel column chromatography, which afforded 2-difluoroacetylimino-3-(3-trifluoromethylphenyl)-5-methylthiazoline (1.01 g, 3.0 mmol, yield 60%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05484933
Quelldatensatzuspto-grants-1996_01
ORD IDord-422c34cb68ba4bdcb5025b23531f5e03
Quellennotizuspto-grants-1996_01