Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
ReactantN-HydroxyphthalimideHCID 10665—
Reactant1,4-DioxaneHCID 31275—
SolventWaterHCID 962—
Product1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl benzoateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115541B2
Source datasetuspto-grants-2006_10
ORD IDord-540120541a7f428a95c9c5e4a4d6067e
Source noteuspto-grants-2006_10