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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421181Generated: November 1, 2026

Indole → 1H-Indole-1-ethanol

https://huagongshe.com/reaction/1421181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantEthylene OxideHCID 6354—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product1H-Indole-1-ethanolHCID 13734996—

Reaction Steps

11.7 g of indole in 500 ml of DMF were treated with 4 g of sodium hydride dispersed in mineral oil. After 1 hour the mixture was cooled in an ice bath and 10 ml of ethylene oxide were added. The mixture was allowed to warm to room temperature and was then stirred for 2 hours. The solvent was evaporated and the residue was treated with 50 ml of water and neutralized with 2M hydrochloric acid. The product was extracted into dichloromethane, the solvent was evaporated and the residue was chromatographed with ethyl acetate/petroleum ether to give 7.6 g of 1-(2-hydroxyethyl)indole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE036736
Source datasetuspto-grants-2000_06
ORD IDord-4d9d47f3e62446b892960a982f80b551
Source noteuspto-grants-2000_06