HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 55584Erstellt: 24. Oktober 2026
Potassium Carbonate → 1-[3,5-Dibromo-4-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]phenyl]ethanone
https://huagongshe.com/de/reaction/55584
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazole | HCID 849421 | — |
| Edukt | 1-[4-(3-Bromopropoxy)-3,5-dibromophenyl]ethanone | HCID 21960118 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 1-[3,5-Dibromo-4-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]phenyl]ethanone | HCID 21960059 | 58,7% |
Reaktionsschritte
A stirred mixture of 6-fluoro-3-(4-piperidinyl)1,2-benzisoxazole (2.0 g, 9.0 mmol), K2CO3 (1.3 g), and 1-[4-(3-bromopropoxy)-3,5-dibromophenyl]ethanone (2.65 g, 9.0 mmol) and acetonitrile (50 ml) was heated at reflux for 3 hours. At the end of the reaction, the solvent was evaporated and the residue was extracted into dichloromethane (150 ml). The insolubles were filtered off. The dichloromethane solution was concentrated down to an oil. The purification was done by flash chromatography on a silica gel column (SiO2, 47 g; eluted with dichloromethane, 300 ml; 1% methanol in dichloromethane, 600 ml). The material thus purified as a colorless oil, solidified on standing. Recrystallization from ethanol gave 1-[3,5-dibromo-4-[3-[4-(6-fluoro-1,2- benzisoxazol-3-yl)-1-piperidinyl]propoxy]-phenyl]ethanone as white crystals (2.93 g, 57%), m.p.=102°-103° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05624927 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-ba28a151c1eb464b9150c76196564cad |
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| Quellennotiz | uspto-grants-1997_04 |
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