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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Epibromohydrin | HCID 18430 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Fluoroindole | HCID 67861 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Fluoro-1-(2-oxiranylmethyl)-1H-indole | HCID 15524200 | 89% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06204274B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-3b2fc20ab0e0475988855526f8b22525 |
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| Source note | uspto-grants-2001_03 |
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