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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantSodium HydroxideHCID 14798—
ReactantPyrrolidineHCID 31268—
Reactant3-(2-bromoethyl)-5-fluoro-1H-indoleHCID 11207226—
Solvent1,4-DioxaneHCID 31275—
Product5-Fluoro-3-(2-(pyrrolidin-1-yl)ethyl)-1H-indoleHCID 49821488—

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138187B2
Source datasetuspto-grants-2012_03
ORD IDord-661c04de31d14ae4b3a2897e9c378f23
Source noteuspto-grants-2012_03