HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 964102Erstellt: 25. Oktober 2026
1H-Isoindole-1,3(2H)-dione, 2-(bromomethyl)- → 2-(Phthalimidomethyloxy)pyridine
https://huagongshe.com/reaction/964102
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1H-Isoindole-1,3(2H)-dione, 2-(bromomethyl)- | HCID 79244 | — |
| Edukt | HCID 178516071 | HCID 178516071 | — |
| Katalysator | HCID 178418647 | HCID 178418647 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | 2-(Phthalimidomethyloxy)pyridine | HCID 19079152 | 39,3% |
Reaktionsschritte
In 4 ml of benzene were suspended 0.095 g (1.0 mmol) of 2-hydroxypyridine and 0.14 g (0.5 mmol) of silver carbonate, N-bromomethylphthalimide [0.29 g (1.2 mmol)] was added at room temperature, and the mixture was stirred at 80° C. for 14 hours under heating. After cooling, the residue was filtered and the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate/hexane=10:1) to obtain powder. The powder was recrystallized from ethyl acetate to obtain 0.10 g of the desired compound (yield: 39.0%, colorless columns).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05767121 |
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| Quelldatensatz | uspto-grants-1998_06 |
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| ORD ID | ord-0963a453584747558468c369c862f080 |
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| Quellennotiz | uspto-grants-1998_06 |
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