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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816124Generated: October 31, 2026

Potassium Carbonate → 1-(6-chloro-1-propyl-1H-indol-3-yl)-2,2,2-trifluoro-ethanone

https://huagongshe.com/reaction/1816124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-IodopropaneHCID 33643—
Reactant1-(6-Chloro-3-indolyl)-2,2,2-trifluoroethanoneHCID 22497252—
SolventDimethylformamideHCID 6228—
Product1-(6-chloro-1-propyl-1H-indol-3-yl)-2,2,2-trifluoro-ethanoneHCID 22497253118.1%

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of 1-(6-chloro-1H-indol-3-yl)-2,2,2-trifluoro-ethanone (200 mg, 0.81 mmol) and potassium carbonate (214 mg, 2.02 mmol) in N,N-dimethylformamide (4 mL) was stirred at 25° C. for 30 min. At this time, the reaction was treated with 1-iodopropane (0.12 mL, 1.21 mmol) and heated at 60° C. for 5 h. The reaction mixture was cooled to 25° C. and then concentrated in vacuo. The residue was diluted with ethyl acetate (50 mL) and was washed with a saturated aqueous sodium bicarbonate solution (1×50 mL), water (2×50 mL) and a saturated aqueous sodium chloride solution (1×50 mL). The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo to afford 1-(6-chloro-1-propyl-1H-indol-3-yl)-2,2,2-trifluoro-ethanone (277.1 mg) as an orange solid which was used without further purification or characterization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06881844B2
Source datasetuspto-grants-2005_04
ORD IDord-c63f149e96e54a13a43b452b9ef69eee
Source noteuspto-grants-2005_04