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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252514Generated: October 25, 2026

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

https://huagongshe.com/reaction/252514

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 numberUS07868037B2
Source datasetuspto-grants-2011_01
ORD IDord-ff3633a85fb14e399d26b5a8775f5ede
Source noteuspto-grants-2011_01