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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | 6-(Trifluoromethoxy)-1H-indole | HCID 22048958 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Ethyl-6-trifluoromethoxyindole-3-carbonitrile | HCID 59425835 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07868037B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-a41d5cb959cc4bfdb6da9ad5d3ec8bae |
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| Source note | uspto-grants-2011_01 |
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