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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532616Generated: October 31, 2026

Water → 5-Fluoro-1-(2-oxiranylmethyl)-1H-indole

https://huagongshe.com/reaction/1532616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEpibromohydrinHCID 18430—
ReactantSodium hydrideHCID 24758—
Reactant5-FluoroindoleHCID 67861—
SolventDimethylformamideHCID 6228—
Product5-Fluoro-1-(2-oxiranylmethyl)-1H-indoleHCID 1552420089%

Reaction Conditions

Temperature60 °C

Reaction Steps

Epibromohydrin (1.4 ml, 16.5 mmole) was added to a stirred solution of 5-fluoroindole (2.0 g, 15 mmole) and sodium hydride (0.66 g, 16.5 mmole) in anhydrous DMF (20 ml), and the mixture was heated at 60° C. under nitrogen for 15 hours. Water (100 ml) was added and the product extracted into CH2Cl2 (3×35 ml). The combined organics were washed with water (25 ml), brine (25 ml) and dried over anhydrous sodium sulfate. Filtration and concentration in vacuo gave the crude product as a viscous yellow colored oil (2.7 g). This was purified by flash silica gel chromatography (30% ethyl acetate in hexane) to afford the titled product as a viscous oil (2.5 g, 89% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06204274B1
Source datasetuspto-grants-2001_03
ORD IDord-3b2fc20ab0e0475988855526f8b22525
Source noteuspto-grants-2001_03