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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 485490Erstellt: 25. Oktober 2026

1-(3-(Trifluoromethyl)phenyl)piperazine → 1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-(3-trifluoromethylphenyl)piperazine hydrochloride

https://huagongshe.com/reaction/485490

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(3-(Trifluoromethyl)phenyl)piperazineHCID 4296—
EduktPotassium IodideHCID 4875—
EduktPotassium CarbonateHCID 11430—
Edukt3-(3-Chloropropyl)-6-fluorobenzo[d]isoxazoleHCID 10910880—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-(3-trifluoromethylphenyl)piperazine hydrochlorideHCID 1352073735,8%

Reaktionsschritte

A mixture of 6.5 g of 3-(3-chloropropyl)-6-fluoro-1,2-benzisoxazole, 5.8 g of N-(α,α,α-trifluoro-m-tolyl)piperazine, 7.0 g of potassium carbonate and a few crystals potassium iodide in 80 ml of dimethylformamide was stirred at 70°-75° C. for seven hrs. The reaction mixture was cooled, filtered and concentrated to an oil, which was stirred with water and extracted with ether-ethyl acetate. The organic extracts were washed with water (2×), saturated sodium chloride solution, and dried over anhydrous magnesium sulfate. The mixture was filtered and concentrated to an oil, which was converted to a salt by treatment with ethereal hydrogen chloride. The salt was recystallized from ethyl acetate/methanol to give 4 g (35%) of product mp, 208°-209° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04536578
Quelldatensatzuspto-grants-1985_08
ORD IDord-50dc8d30fd9d4f23a8e58a21a5c42f11
Quellennotizuspto-grants-1985_08