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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532338Generated: October 31, 2026

Iodoethane → Ethyl 6-cyano-1-ethylindole-2-carboxylate

https://huagongshe.com/reaction/1532338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 6-cyano-1H-indole-2-carboxylateHCID 4715002—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductEthyl 6-cyano-1-ethylindole-2-carboxylateHCID 21251527—

Reaction Steps

In a 1 l flask, 23.5 g of ethyl 6-cyanoindole-2-carboxylate was dissolved in 300 ml of dimethylformamide, and 6.6 g of 60% NaH was slowly added thereto at 0° C. 17.6 ml of iodoethane was then added thereto at −10˜0° C. and the mixture was stirred for 2 hours at room temperature. The reaction solution was cooled and, after adding ice, diluted with water and then extracted three times with ethyl acetate. The organic extracts were combined, dried over MgSO4 and then evaporated. The residue was purified with silica gel column chromatography [eluent: ethyl acetate/n-hexane(1:3)]. The fractions containing the desired product were combined and then evaporated to obtain 26.2 g of the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06201006B1
Source datasetuspto-grants-2001_03
ORD IDord-dc3e2711508f48df8b3988d06646cca6
Source noteuspto-grants-2001_03