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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506021Generated: October 27, 2026

Iodoethane → 1-ethyl-6-methoxy-2-methyl-1H-indole-3-carbonitrile

https://huagongshe.com/reaction/506021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
Reactant6-methoxy-2-methyl-1H-indole-3-carbonitrileHCID 13904640—
SolventDimethylformamideHCID 6228—
Product1-ethyl-6-methoxy-2-methyl-1H-indole-3-carbonitrileHCID 5942526592%

Reaction Steps

To a suspension of NaH (0.6 g, 2 eq.) in DMF (7 mL) is added a solution of 6-methoxy-2-methyl-1H-indole-3-carbonitrile (1.3 g, 7.0 mmol) in DMF (8 mL) followed by ethyl iodide (1.2 mL, 2 eq.) at 0° C. After stirring for 1 h, the mixture is poured into ice water and then extracted with CH2Cl2. The organic layer is washed with brine and dried with Na2SO4. The solvent is evaporated under vacuum and purified with flash column chromatography on silica gel using EtOAc/petroleum ether (1/5) as eluent to yield 92% of 1-ethyl-6-methoxy-2-methyl-1H-indole-3-carbonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781478B2
Source datasetuspto-grants-2010_08
ORD IDord-c972adf366224ac1964d1f2fb3305c0d
Source noteuspto-grants-2010_08