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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-3-methylbutane | HCID 7891 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(6-Chloro-3-indolyl)-2,2,2-trifluoroethanone | HCID 22497252 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22497219 | HCID 22497219 | 110.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06881844B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-a99721f950ab40ab90e1f7ad5f9a3f7b |
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| Source note | uspto-grants-2005_04 |
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