Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890842Generated: October 26, 2026

Pyridine → 4-dodecyloxycarbonyl-N-hydroxyphthalimide

https://huagongshe.com/reaction/890842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant4-Dodecyloxycarbonylphthalic anhydrideHCID 606385—
SolventWaterHCID 962—
Product4-dodecyloxycarbonyl-N-hydroxyphthalimideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06998491B2
Source datasetuspto-grants-2006_02
ORD IDord-2470230dec804fdd8c4ea3cbfda3454c
Source noteuspto-grants-2006_02