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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186032Generated: November 2, 2026

2-(2-Bromo-4,5-dimethoxy-benzyl)isoindole-1,3-dione → 2-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-4,5-dimethoxy-benzonitrile

https://huagongshe.com/reaction/1186032

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-Bromo-4,5-dimethoxy-benzyl)isoindole-1,3-dioneHCID 8865707—
ReactantHCID 178418546HCID 178418546—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product2-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-4,5-dimethoxy-benzonitrileHCID 67188766—

Reaction Steps

A mixture of 2-(2-bromo-4,5-dimethoxy-benzyl)isoindole-1,3-dione (26.63 g, 0.07079 mol) and copper (I) cyanide (12.7 g, 0.1416 mol) in N-methyl-2-pyrrolidinone (266 mL) was heated to reflux for 18 h under nitrogen. The resulting mixture was concentrated in vacuo and the resulting residue stirred with a mixture of chloroform (250 mL) and water (250 mL) for 30 min. The resulting suspension was filtered through CELITE and the layers separated. The organic layer was extracted with brine (2×), dried over MgSO4, filtered and concentrated in vacuo. The resulting solid was crystallized from methylene chloride/methanol (500 mL) to yield 2-(1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-4,5-dimethoxy-benzonitrile as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673890B2
Source datasetuspto-grants-2014_03
ORD IDord-19646c43804c4ab4a6bfab40820a7fc6
Source noteuspto-grants-2014_03