HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890842Generated: October 26, 2026
Pyridine → 4-dodecyloxycarbonyl-N-hydroxyphthalimide
https://huagongshe.com/reaction/890842
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 4-Dodecyloxycarbonylphthalic anhydride | HCID 606385 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-dodecyloxycarbonyl-N-hydroxyphthalimide | HCID 10915765 | — |
Reaction Steps
In a 500-ml flask equipped with a stirrer, a thermometer and a dropping funnel, 100 g (277.43 mmol) of 4-dodecyloxycarbonylphthalic anhydride, 21.21 g (305.17 mmol) of hydroxylamine hydrochloride and 250 g of pyridine were placed and were stirred at room temperature in an atmosphere of nitrogen gas for 30 minutes, followed by stirring at 90° C. for further 3 hours. The resulting reaction mixture was added dropwise to 3000 g of pure water over 30 minutes with stirring and thereby yielded a crystal of 4-dodecyloxycarbonyl-N-hydroxyphthalimide. The mixture was stirred for further 1 hour, the precipitate was separated by filtration and was rinsed with pure water. The resulting solid was stirred and rinsed in a solvent mixture of 640 g of n-hexane and 160 g of ethyl acetate for 3 hours, the resulting slurry was filtrated, was rinsed with n-hexane, was dried at 60° C. under reduced pressure and thereby yielded 90.88 g (242.04 mmol) of target 4-dodecyloxycarbonyl-N-hydroxyphthalimide as a white powder. The yield was 87.2% on the basis of 4-dodecyloxycarbonylphthalic anhydride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06998491B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-2470230dec804fdd8c4ea3cbfda3454c |
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| Source note | uspto-grants-2006_02 |
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