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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907121Generated: October 30, 2026

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

https://huagongshe.com/reaction/907121

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) was 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 was poured into ice water and the extracted with CH2Cl2. The organic layer was washed with brine and dried with Na2SO4. The solvent was 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 numberUS08013006B2
Source datasetuspto-grants-2011_09
ORD IDord-bdfe014327f743f0ba8b0e9e6530ca33
Source noteuspto-grants-2011_09