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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(6-Chloro-3-indolyl)-2,2,2-trifluoroethanoneHCID 22497252—
SolventDimethylformamideHCID 6228—
Product1-[6-Chloro-1-(1-methylethyl)-1H-indol-3-yl]-2,2,2-trifluoroethanoneHCID 2249725483%

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06881844B2
Source datasetuspto-grants-2005_04
ORD IDord-bec589cf7d3d4a619254f2ec8ca05134
Source noteuspto-grants-2005_04