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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884822Generated: November 1, 2026

Ethyl Bromide → 1-Ethyl-1H-indole-3-carbaldehyde

https://huagongshe.com/reaction/1884822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantIndole-3-CarboxaldehydeHCID 10256—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product1-Ethyl-1H-indole-3-carbaldehydeHCID 59909080%

Reaction Steps

1-ethylindole-3-carboxaldehyde was prepared from alkylation reaction of indole-3-carboxaldehyde. Indole-3-carboxaldehyde (900 mg, 6.2 mmol) was dissolved in 5 ml dimethylformamide, ethyl bromide (918 μl, 12 mmol) and sodium hydride (282.8 mg, 12 mmol) were added to the reaction mixture. Solution was stirred and refluxed for three hours. The reaction mixture was then evaporated to dryness and washed with water. Pale brown crystals were obtained with 80% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06767909B2
Source datasetuspto-grants-2004_07
ORD IDord-40882a553ceb4b4b93ed98acb4a6c827
Source noteuspto-grants-2004_07