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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816092Generated: October 30, 2026

Isopropyl iodide → HCID 22497250, compound

https://huagongshe.com/reaction/1816092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 22497232HCID 22497232—
SolventDimethylformamideHCID 6228—
ProductHCID 22497250HCID 2249725074%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 2,2,2-trifluoro-1-(6-trifluoromethyl-1H-indol-3-yl)-ethanone (1.0 g, 3.56 mmol) in N,N-dimethylformamide (10 mL) at 25° C. was treated with potassium carbonate (1.22 g, 8.89 mmol). The resulting mixture was stirred at 25° C. for 10 min. At this time, the reaction was treated with 2-iodopropane (0.53 mL, 5.34 mmol). The reaction was heated at 65° C. for 4 h. At this time, the reaction was cooled to 25° C. and was partitioned between water (75 mL) and ethyl acetate (75 mL). The organic layer was washed with a 1N aqueous hydrochloric acid solution (1×25 mL), water (1×50 mL), and a saturated aqueous sodium chloride solution (1×50 mL). The organic layer was then dried over magnesium sulfate, filtered, and concentrated in vacuo to afford 2,2,2-trifluoro-1-(1-isopropyl-6-trifluoromethyl-1H-indol-3-yl)-ethanone (850 mg, 74%) as a pale orange solid: mp 92-93° C.; EI-HRMS m/e calcd for C14H11F6NO (M+) 323.0745, found 323.0739.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06881844B2
Source datasetuspto-grants-2005_04
ORD IDord-75cc6be65a744f46ad68b5968b78e954
Source noteuspto-grants-2005_04