Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564446Generated: October 30, 2026

Dimethylformamide → 2-[(3-bromo-5-methylphenyl)methyl]-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/564446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant1-Bromo-3-(bromomethyl)-5-methylbenzeneHCID 22324261—
ReactantPotassium phthalideHCID 67006573—
Product2-[(3-bromo-5-methylphenyl)methyl]-1H-isoindole-1,3(2H)-dioneHCID 5781344167%

Reaction Steps

To a solution of 1-bromo-3-(bromomethyl)-5-methylbenzene (34.0 g, 128.8 mmol) in DMF (200 mL), was added potassium phthalide (28.9 g, 154.6 mmol), and the mixture was stirred under reflux for 2 h. The reaction was allowed to cool to room temperature. After the solvent was remove under reduced pressure, the residue was dissolved in CH2Cl2 (300 mL), and washed with water (50 mL×3). The organic layer was dried over anhydrous sodium sulfate. Evaporation of the solvent gave a white solid. The solid was recrystallized from toluene and EtOH to give the product, 2-[(3-bromo-5-methylphenyl)methyl]-1H-isoindole-1,3(2H)-dione (28.5 g, 67%). 1H NMR (400 MHz, CDCl3): δ 7.87-7.72 (m, 4 H), 7.36 (s, 1H), 7.23 (s, 1 H), 7.15 (s, 1 H), 4.77 (s, 2 H), 2.30 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067408B2
Source datasetuspto-grants-2011_11
ORD IDord-d3361df022ff41b998f0dc64a9effee9
Source noteuspto-grants-2011_11