HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095520Generated: November 2, 2026
Chloroform → 5-Fluoro-3-(2-(pyrrolidin-1-yl)ethyl)-1H-indole
https://huagongshe.com/reaction/1095520
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 3-(2-bromoethyl)-5-fluoro-1H-indole | HCID 11207226 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-Fluoro-3-(2-(pyrrolidin-1-yl)ethyl)-1H-indole | HCID 49821488 | — |
Reaction Steps
Pyrrolidine (2.94 g, 3.4 ml, 41.3 mmol) was dissolved in abs dioxane (100 ml), 3-(2-bromo-ethyl)-5-fluoro-1H-indole (5.00 g, 20.7 mmol) was added at RT and the mixture was stirred at 70° C. for 8 h. The solution was concentrated, the residue was taken up in CHCl3 (150 ml) and the mixture was washed with water (2×50 ml). The organic phase was dried over Na2SO4, filtered and concentrated i. vac. The residue obtained was purified by flash chromatography with 500 g of silica gel and chloroform/methanol (20:1→9:1→4:1→methanol. Only with methanol was a salt of the compound obtained, and it was then possible to liberate this by stirring with 2N NaOH and CHCl3. The phases were separated, the aqueous phase was extracted twice with CHCl3 and the combined organic phases were dried over Na2SO4, filtered and concentrated i. vac. The chloroform used was probably contaminated with HCl.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138187B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-661c04de31d14ae4b3a2897e9c378f23 |
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| Source note | uspto-grants-2012_03 |
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