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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252595Generated: October 25, 2026

Iodoethane → 1-Ethyl-6-trifluoromethoxyindole-3-carbonitrile

https://huagongshe.com/reaction/252595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
ReactantChlorosulfonyl isocyanateHCID 70918—
Reactant6-(Trifluoromethoxy)-1H-indoleHCID 22048958—
SolventDimethylformamideHCID 6228—
Product1-Ethyl-6-trifluoromethoxyindole-3-carbonitrileHCID 5942583586%

Reaction Steps

To a solution of 6-trifluoromethoxyindole (2.68 g, 13.3 mmol) in dry DMF (10 mL) at 0° C., is added chlorosulfonylisocyanate (2.35 g, 1.44 mL, 16.6 mmol). The mixture is then brought to room temperature slowly and stirred for 1 h. The mixture is poured into ice (100 mL) and stirred for 1 h. The precipitate is collected by filtration and washed thoroughly with water and dried in vacuo, which is then dissolved in DMF (15 mL). To the solution is added K2CO3 and EtI (2.59 g, 1.34 mL, 16.6 mmol), and the mixture is stirred at 50° C. overnight. It is then poured into ice-water (200 mL). The precipitate is collected by filtration and washed with water, dried in air and purified by chromatography (silica gel, DCM) to furnish 1-ethyl-6-trifluoromethoxyindole-3-carbonitrile (2.90 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868037B2
Source datasetuspto-grants-2011_01
ORD IDord-a41d5cb959cc4bfdb6da9ad5d3ec8bae
Source noteuspto-grants-2011_01