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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2452Generated: October 23, 2026

Sodium Iodide → 4-[(1,3-dioxoisoindol-2-yl)methyl]-N-(2-methoxyphenyl)benzamide

https://huagongshe.com/en/reaction/2452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPhthalimideHCID 6809—
ReactantSodium hydrideHCID 24758—
Reactant4-Chloromethyl-N-(2-methoxyphenyl)benzamideHCID 19689968—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product4-[(1,3-dioxoisoindol-2-yl)methyl]-N-(2-methoxyphenyl)benzamideHCID 299452077.6%

Reaction Steps

In an atmosphere of argon, phthalimide (150 mg, 1.0 mmol) was dissolved in THF (10 ml) to which was subsequently added sodium hydride (44 mg, 60%, 1.1 mmol) at room temperature. After 40 minutes of stirring at the same temperature, to this was added a DMF solution (5 ml) containing 4-chloromethyl-N-(2-methoxyphenyl)benzamide (276 mg, 1.0 mmol) and a catalytically effective amount of sodium iodide. After 2 hours of stirring at 80° C. and subsequent removal of the solvent by evaporation, the resulting residue was mixed with water (10 ml) and extracted with an ethyl acetate-methylene chloride (1:2) mixture solution. The resulting organic layer was washed with water and saturated brine and dried on anhydrous magnesium sulfate. Thereafter, the solvent was removed by evaporation, and the resulting residue was subjected to a silica gel column chromatography (methylene chloride-ether:hexane=2:1) and then washed with ether to obtain 300 mg (77.6%) of the title compound in the form of colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728835
Source datasetuspto-grants-1998_03
ORD IDord-0629cd8f2ed34187aae991fef93b63da
Source noteuspto-grants-1998_03