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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009637Generated: October 25, 2026

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

https://huagongshe.com/reaction/1009637

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 numberUS07973069B2
Source datasetuspto-grants-2011_07
ORD IDord-a0ed4a77f81b48e58b1523a4d64344de
Source noteuspto-grants-2011_07