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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 235408Erstellt: 24. Oktober 2026

Potassium Carbonate → 2-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]methyl-1,4-benzodioxan

https://huagongshe.com/de/reaction/235408

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt2,3-Dihydro-1,4-benzodioxin-2-ylmethyl methanesulfonateHCID 263445—
Edukt3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
LösungsmittelAcetonitrileHCID 6342—
Produkt2-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]methyl-1,4-benzodioxanHCID 15384968—

Reaktionsschritte

A stirred mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole (3.0 g, 13.6 mmol), K2CO3 (2.45 g, 17.7 mmol), 2-methanesulfonyloxymethyl-1,4-benzodioxan (3.35 g, 13.7 mmole) in acetonitrile (100 ml) was heated at reflux for 12 hours. At the end of the reaction, the insolubles were filtered and rinsed with dichloromethane. The organic solution was concentrated. The crude oil was purified by flash chromatography on a silica gel column. The fractions containing the pure product were pooled and concentrated to a light yellow oil (3.94 g, 74%). Crystallization from ethanol and petroleum ether gave 2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]methyl-1,4-benzodioxan as off-white crystals, 2.22 g, m.p.=86°-87° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05597842
Quelldatensatzuspto-grants-1997_01
ORD IDord-d7d25dc35f2846929290194e1d7ebff7
Quellennotizuspto-grants-1997_01