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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628458Generated: November 1, 2026

Chlorosuccinimide → 1-Allyl-4-chloro-7-(1-ethylpropyl)-1,3-dihydro-2H-benzimidazol-2-one

https://huagongshe.com/reaction/1628458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
Reactant1-Allyl-7-(1-ethylpropyl)-1,3-dihydro-2H-benzimidazol-2-oneHCID 68770712—
CatalystZirconium chloride (ZrCl4), (T-4)-HCID 9856075—
SolventTolueneHCID 1140—
Product1-Allyl-4-chloro-7-(1-ethylpropyl)-1,3-dihydro-2H-benzimidazol-2-oneHCID 6877112938.3%

Reaction Steps

To a mixture of 1-allyl-7-(1-ethylpropyl)-1,3-dihydro-2H-benzimidazol-2-one (22.0 g, 89.8 mmol) and zirconium chloride (1.05 g, 4.49 mmol) in toluene (300 mL) was added N-chlorosuccinimide (12.4 g, 92.5 g) portionwise at 0° C. After stirring for 15 hr, the mixture was concentrated in vacuo to give a residue which was partitioned in aqueous sodium bicarbonate and ethyl acetate. The aqueous layer was extracted with ethyl acetate. Combined organic layer was washed with aqueous sodium bicarbonate and brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was dissolved in hot ethyl acetate. n-Hexane was then added and the solution was cooled down. Resulting precipitate was collected by filtration to afford the title compound (9.60 g, 34.4 mmol, 38%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785460B2
Source datasetuspto-grants-2014_07
ORD IDord-b8287fe0c01340a5b41a531eb81bd547
Source noteuspto-grants-2014_07