HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241252Generated: October 25, 2026
Pyridine → 1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl benzoate
https://huagongshe.com/reaction/1241252
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl benzoate | HCID 792579 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07115541B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-540120541a7f428a95c9c5e4a4d6067e |
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| Source note | uspto-grants-2006_10 |
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