HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18855Erstellt: 23. Oktober 2026
Pyridine → 1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl benzoate
https://huagongshe.com/de/reaction/18855
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Benzoyl chloride | HCID 7412 | — |
| Edukt | N-Hydroxyphthalimide | HCID 10665 | — |
| Edukt | 1,4-Dioxane | HCID 31275 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl benzoate | HCID 792579 | — |
Reaktionsschritte
In a 3-L flask equipped with a stirrer and thermometer, 100 g (613 mmol) of N-hydroxyphthalimide, 53.3 g (674 mmol) of pyridine and 1100 g of 1,4-dioxane were placed and were stirred at room temperature. To the resulting mixture, 94.8 g (674 mmol) of benzoyl chloride was added dropwise over 1 hour, and the resulting mixture was stirred at room temperature for further 2 hours. Subsequently, 1100 g of pure water was added dropwise over 30 minutes to dissolve by-produced salts and thereby yielded a crystal of the target N-benzoyloxyphthalimide. The mixture was stirred and aged for further 1 hour, the crystal was filtrated using a Nutsche, was rinsed with an appropriate amount of water, was dried at 60° C. under a reduced pressure and thereby yielded 162 g (604 mmol) of N-benzoyloxyphthalimide in a yield of 98.6% on the basis of N-hydroxyphthalimide.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07741514B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-7125f8827f364b5e9510808c06f203bd |
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| Quellennotiz | uspto-grants-2010_06 |
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