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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362968Generated: October 31, 2026

1-Bromo-3-chloropropane → 1-(3-Chloropropyl)-3,3-difluoroindolin-2-one

https://huagongshe.com/reaction/2362968

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantSodium hydrideHCID 24758—
Reactant3,3-Difluoroindolin-2-oneHCID 5323821—
SolventDimethylformamideHCID 6228—
Product1-(3-Chloropropyl)-3,3-difluoroindolin-2-oneHCID 58046616100.3%

Reaction Steps

A solution of 3,3-difluoroindolin-2-one (836.6 mg, 4.95 mmol, 1 equiv) in N,N-dimethylformamide was cooled to 0° C. Sodium hydride (60% dispersion) (217.6 mg, 5.44 mmol, 1.1 equiv) was slowly added and the reaction was stirred as such until all bubbling had stopped. 1-bromo-3-chloropropane (1.46 ml, 14.85 mmol, 3 equiv) was added to the reaction mixture in one portion. The reaction was allowed to warm to ambient temperature and stirred as such for 16 h. The crude mixture was partitioned between ethyl acetate and water. The organic layer was dried over MgSO4, filtered, concentrated, and the residue was purified using the Biotage flash chromatography system (SNAP 50 g cartridge, Rf=0.5, gradient—5%-30% ethyl acetate in hexanes) to afford the title compound as a yellow oil (1.22 g, quant); MS for C11H10ClF2NO m/z 247.01 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691836B2
Source datasetuspto-grants-2014_04
ORD IDord-44a874f02d6444d5a552590e7801e90b
Source noteuspto-grants-2014_04