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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816132Generated: November 3, 2026

1-Bromo-3-methylbutane → HCID 22497219, compound

https://huagongshe.com/reaction/1816132

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-methylbutaneHCID 7891—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(6-Chloro-3-indolyl)-2,2,2-trifluoroethanoneHCID 22497252—
SolventDimethylformamideHCID 6228—
ProductHCID 22497219HCID 22497219110.7%

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 (2 mL) was stirred at 25° C. for 30 min. This mixture was then treated with 1-bromo-3-methylbutane (0.15 mL, 1.21 mmol) and then heated at 60° C. for 5 h. At this time, the reaction was cooled to 25° C. and 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 sodium sulfate, filtered, and concentrated in vacuo to afford 1-[6-chloro-1-(3-methyl-butyl)-1H-indol-3-yl]-2,2,2-trifluoro-ethanone (284.9 mg) as dark yellow 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-a99721f950ab40ab90e1f7ad5f9a3f7b
Source noteuspto-grants-2005_04