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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595929Generated: October 31, 2026

Imidazole → 2-fluoro-5-(4-(iodomethyl)tetrahydro-2H-pyran-4-yl)pyridine

https://huagongshe.com/reaction/595929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
Reactant(4-(6-fluoropyridin-3-yl)tetrahydro-2H-pyran-4-yl)methanolHCID 118045465—
SolventDichloromethaneHCID 6344—
Product2-fluoro-5-(4-(iodomethyl)tetrahydro-2H-pyran-4-yl)pyridineHCID 11804522460.6%

Reaction Steps

To an ice cooled solution of triphenylphosphine (983 mg, 3.75 mmol), iodine (952 mg, 3.75 mmol) in dichloromethane (20 mL) was added imidazole (278 mg, 4.09 mmol). The solution was stirred at ambient temperature for 1 h, followed by the addition of (4-(6-fluoropyridin-3-yl)tetrahydro-2H-pyran-4-yl)methanol (360 mg, 1.70 mmol) in 10 mL dichloromethane. The reaction mixture was heated to 60° C. in an oil bath for 48 h. Solid was filtered off, the filtrate was purified by flash column chromatography on silicagel (ISCO) eluting with 0-80% ethyl acetate in heptane to give to give 2-fluoro-5-(4-(iodomethyl)tetrahydro-2H-pyran-4-yl)pyridine (330 mg, 1.03 mmol, 60.3% yield) as light yellow color oil. LCMS (m/z): 322 (MH+), 0.77 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-e518d87dac2c480bbca8c40730fb90c5
Source noteuspto-grants-2016_01