HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816152Generated: October 31, 2026
Isopropyl iodide → 1-[6-Chloro-1-(1-methylethyl)-1H-indol-3-yl]-2,2,2-trifluoroethanone
https://huagongshe.com/reaction/1816152
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(6-Chloro-3-indolyl)-2,2,2-trifluoroethanone | HCID 22497252 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[6-Chloro-1-(1-methylethyl)-1H-indol-3-yl]-2,2,2-trifluoroethanone | HCID 22497254 | 83% |
Reaction Steps
A solution of 1-(6-chloro-1H-indol-3-yl)-2,2,2-trifluoro-ethanone in N,N-dimethylformamide (5 mL) was treated with potassium carbonate (698 mg, 5.05 mmol). The reaction was stirred at 25° C. for 15 min and then was treated with 2-iodopropane (0.30 mL, 3.03 mmol). This mixture was heated at 65° C. for 20 h. At this time, the reaction was cooled to 25° C., quenched with water (5 mL), and then partitioned between water (50 mL) and ethyl acetate (50 mL). This mixture was treated with a saturated aqueous sodium chloride solution (1×25 mL), shaken, and separated. The organic layer was then dried over magnesium sulfate, filtered, and concentrated in vacuo. Biotage chromatography (FLASH 40M, Silica, 3/1 hexanes/ethyl acetate) afforded 1-(6-chloro-1-isopropyl-1H-indol-3-yl)-2,2,2-trifluoro-ethanone (483 mg, 83%) as a pale pink solid: mp 94-96° C.; EI-HRMS m/e calcd for C13H11ClF3NO (M+) 289.0481, found 289.0482.
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-bec589cf7d3d4a619254f2ec8ca05134 |
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| Source note | uspto-grants-2005_04 |
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