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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345694Generated: November 2, 2026

Indole → 1H-Indole-1-ethanol

https://huagongshe.com/reaction/345694

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 numberUS05057614
Source datasetuspto-grants-1991_10
ORD IDord-e2bda155152b445b84b8abb4b2d27f90
Source noteuspto-grants-1991_10