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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502106Generated: October 26, 2026

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

https://huagongshe.com/reaction/502106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
Reactant6-Methoxy-1H-indole-3-carbonitrileHCID 53401197—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-ethyl-6-methoxy-1H-indole-3-carbonitrileHCID 11644100—

Reaction Steps

To a solution of 6-methoxy-1H-indole-3-carbonitrile (9.9 g, 57.6 mmol) in DMF (150 mL) is added NaH (60% dispersion in mineral oil, 3.45 g, 86.3 mmol). The reaction mixture is stirred for 15 min and then ethyl iodide (5.53 mL, 69.1 mmol) is added and the mixture is stirred at room temperature overnight. The reaction mixture is then diluted with H2O and extracted with EtOAc (2×). The organic phases are washed with H2O (3×) and saturated NaCl and then dried and concentrated to a semi-solid. The crude product is purified via column chromatography on silica gel (200 g) using CH2Cl2/hexanes (50-100%) as eluent to yield 6-methoxy-1-ethyl-1H-indole-3-carbonitrile as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772271B2
Source datasetuspto-grants-2010_08
ORD IDord-c05e57aeb81c4ee2964fe72c0ac1ca47
Source noteuspto-grants-2010_08