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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489788Generated: October 26, 2026

2-Butene, 1,4-dibromo- → 2-(4-Bromobut-2-en-1-yl)-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/1489788

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butene, 1,4-dibromo-HCID 13180—
ReactantPhthalimide potassium saltHCID 24194345—
SolventDimethylformamideHCID 6228—
Product2-(4-Bromobut-2-en-1-yl)-1H-isoindole-1,3(2H)-dioneHCID 5342343274%

Reaction Steps

Potassium phthalimide (4.60 g, 24.8 mmol) was added in four portions at 15-min intervals to a solution of 1,4-dibromo-2-butene (10.60 g, 49.5 mmol) in dimethylformamide (20 mL) and the resulting mixture was stirred overnight at room temperature. The mixture was concentrated under reduced pressure and the residue was partitioned between dichloromethane (25 mL) and 2N aqueous hydrochloric acid (25 mL). The aqueous layer was-extracted with dichloromethane (2×25 mL) and the organic layers were washed in succession with saturated aqueous sodium chloride (20 mL), dried (sodium sulfate), filtered, and evaporated. The crude product was purified by flash column chromatography silica gel (150 g) eluting with 50% dichlormethane/hexane increasing to 100% dichlormethane to yield 5.12 g (74% yield) of white crystalline product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05679700
Source datasetuspto-grants-1997_10
ORD IDord-7e8b88c842b5499c924b83ff44c71130
Source noteuspto-grants-1997_10