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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816102Generated: November 1, 2026

Isopropyl iodide → HCID 22497220, compound

https://huagongshe.com/reaction/1816102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 22497238HCID 22497238—
SolventDimethylformamideHCID 6228—
ProductHCID 22497220HCID 2249722085%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 2,2,2-trifluoro-1-(6-methoxy-1H-indol-3-yl)-ethanone (1.0 g, 4.11 mmol) in N,N-dimethylformamide (10 mL) at 25° C. was treated with potassium carbonate (1.42 mg, 10.28 mmol). The resulting mixture was stirred at 25° C. for 30 min and then was treated with 2-iodopropane (0.62 mL, 6.17 mmol). The reaction was heated at 65° C. for 20 h. At this time, the reaction was cooled to 25° C. and was partitioned between water (50 mL) and ethyl acetate (50 mL). This mixture was treated with a 1N aqueous hydrochloric acid solution (25 mL), shaken, and separated. The organic layer was washed with water (1×50 mL) and a saturated aqueous sodium chloride solution (1×50 mL), dried over magnesium sulfate, filtered, and concentrated in vacuo. Biotage chromatography (FLASH 40M, Silica, 3/1 hexanes/ethyl acetate) afforded 2,2,2-trifluoro-1-(1-isopropyl-6-methoxy-1H-indol-3-yl)-ethanone (99 mg, 85%) as a yellow solid: mp 58-60° C.; EI-HRMS m/e calcd for C14H14F3NO2 (M+) 285.0977, found 285.0974.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06881844B2
Source datasetuspto-grants-2005_04
ORD IDord-131af04f3cec4dbdaea89abebcde18ae
Source noteuspto-grants-2005_04