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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502140Generated: October 25, 2026

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

https://huagongshe.com/reaction/502140

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 the mixture is 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 numberUS07772271B2
Source datasetuspto-grants-2010_08
ORD IDord-413600d2815f430e94eadbcb4d9b9f25
Source noteuspto-grants-2010_08