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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751041Generated: October 28, 2026

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

https://huagongshe.com/reaction/1751041

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 numberUS09156840B2
Source datasetuspto-grants-2015_10
ORD IDord-61e6303645ed4c288e2fbe0b9d36684f
Source noteuspto-grants-2015_10