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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365850Generated: October 26, 2026

Potassium Iodide → 5-fluoro-4-iodo-1H-indole

https://huagongshe.com/reaction/1365850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantDichloromethaneHCID 6344—
ReactantThallium(III) trifluoroacetateHCID 90200—
ReactantMethyl 5-fluoro-1H-indole-3-carboxylateHCID 34176452—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTrifluoroacetic acidHCID 6422—
Product5-fluoro-4-iodo-1H-indoleHCID 5915129239%

Reaction Steps

A solution of thallium tris(trifluoroacetate) (8.45 g, 15.6 mmol) in TFA (35 mL) was added to a solution of 5-fluoro-1H-indole-3-carboxylic acid methyl ester (2 g, 10.4 mmol) in TFA (10 mL) at room temperature and stirred for 2 h. The reaction mixture was evaporated in vacuo and the resulting residue suspended in water (25 mL) before being treated with a solution of potassium iodide (5.2 g, 31.3 mmol) in water (50 mL). The reaction mixture was treated with dichloromethane (100 mL) and methanol (5 mL) and the resulting precipitate removed by filtration through celite. The organic layer was separated, washed successively with sodium thiosulfate solution and brine, then dried (MgSO4) and evaporated in vacuo. The resultant material was dissolved in methanol (60 mL) and treated with 40% aqueous NaOH solution (60 mL) then refluxed for 2 h. The reaction mixture was cooled to RT and extracted with DCM/MeOH (ratio 95:5). The organic layer was dried (MgSO4), filtered and concentrated in vacuo. The resultant residue was purified by column chromatography (silica gel, pentane:EtOAc 75:25) to provide 5-fluoro-4-iodo-1H-indole as a pale brown solid (1.05 g, 39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893060B2
Source datasetuspto-grants-2011_02
ORD IDord-f22bcef3425e4b5cbb04831b8908b9a2
Source noteuspto-grants-2011_02