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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039539Generated: October 27, 2026

N-Hydroxyphthalimide → 2-(5-Bromo-pyridin-2-ylmethoxy)-isoindole-1,3-dione

https://huagongshe.com/reaction/1039539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-HydroxyphthalimideHCID 10665—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Bromo-2-(chloromethyl)pyridine hydrochlorideHCID 53438200—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product2-(5-Bromo-pyridin-2-ylmethoxy)-isoindole-1,3-dioneHCID 6901101896.5%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a mixture of 5-Bromo-2-chloromethyl-pyridine hydrochloride (63.7 g, 0.262 mol) and N-hydroxylphthalimide (64 g, 0.393 mol) in acetonitrile (400 mL) was placed in water bath and added N,N-diisopropylethylamine (182 mL, 1.05 mol) using dropping funnel for 10 min. It was heated at 65° C. for 4 hrs and evaporated off the solvent and extra base. Then, water (100 mL) was added to the reaction mixture and stirred for overnight. The resulting solid was filtered, washed with water (2×50 mL) and acetonitrile (100 mL). The white solid was dried on vacuum pump to provide the title compound (84.2 g, 84%) as a white solid. MS-ESI m/z 334.95 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552162B2
Source datasetuspto-grants-2013_10
ORD IDord-308d4370c26e4744a0e98d01ea3655b9
Source noteuspto-grants-2013_10