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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640890Generated: November 1, 2026

Iodine → 2-Fluoro-4-iodo-5-(methoxymethoxy)pyridine

https://huagongshe.com/reaction/1640890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantWaterHCID 962—
ReactantHCID 66738421HCID 66738421—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
Product2-Fluoro-4-iodo-5-(methoxymethoxy)pyridineHCID 6673815353%

Reaction Steps

Cool a solution of 2-fluoro-5-methoxymethoxy-pyridine (4.1 g, 26.1 mmol) in THF (60 mL) to −75° C. Add tert-butyllithium (1.7 M in pentane, 30.4 mL, 51.7 mmol) over a period of 30 min. Stir the mixture for an additional half an hour. Add iodine (9.8 g, 38.6 mmol, dissolved in 60 mL of THF). Stir for 1 h after the addition is complete. Allow the temperature to raise to RT over 1 h while stirring. Treat the mixture with water. Extract the solution with ethyl acetate three times. Wash the organic layer with aqueous saturated sodium chloride. Dry the mixture over sodium sulfate. Concentrate the solution in vacuo to a brown solid. Triturate the brown solid with hexane. Filter to afford the title compound (3.9 g, 53%) as a brown solid. 1H NMR (400 MHz, CDCl3) δ 3.53 (s, 3H), 5.23 (s, 2H), 7.39 (d, J=4.0 Hz, 1H), 7.96 (d, J=1.6 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114872B2
Source datasetuspto-grants-2012_02
ORD IDord-40618a1aa80c4a0ca16e648ad66047d6
Source noteuspto-grants-2012_02