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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093150Generated: November 1, 2026

Iodine → Tert-butyl 4-(2-fluoro-5-iodo-4-methoxyphenyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2093150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantTert-butyl 4-(2-fluoro-4-methoxyphenyl)piperidine-1-carboxylateHCID 67066012—
CatalystHCID 178418844HCID 178418844—
SolventMethanolHCID 887—
ProductTert-butyl 4-(2-fluoro-5-iodo-4-methoxyphenyl)piperidine-1-carboxylateHCID 67066021—

Reaction Steps

A stirred mixture of tert-butyl 4-(2-fluoro-4-methoxyphenyl)piperidine-1-carboxylate (Step A; 255 mg; 0.825 mmol) in MeOH (15 mL) was treated with iodine (345 mg; 1.107 mmol) and silver sulfate (281 mg; 1.107 mmol). The reaction was stirred at room temperature for 2 h. The reaction was filtered through Celite and the filtrate was concentrated in vacuo. The residue was redissolved in ether (50 mL) and washed with H2O (50 mL). The aqueous layer was extracted with ether (3×50 mL) and the combined extracts were washed with brine (50 mL), dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by flash silica gel chromatography (0-10% EtOAc/hexanes gradient) to afford tert-butyl 4-(2-fluoro-5-iodo-4-methoxyphenyl)piperidine-1-carboxylate as a colorless glass. The aqueous layer was then re-extracted with EtOAc (3×100 mL) and the combined extracts were dried (MgSO4), filtered, and the solvent was removed under reduced pressure until a precipitate formed. This solid was collected by filtration and dried in a vacuum oven to afford 4-(2-fluoro-5-iodo-4-methoxyphenyl)piperidine as a off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440702B2
Source datasetuspto-grants-2013_05
ORD IDord-6244faef94db4b2a9d1e4860677ddb6e
Source noteuspto-grants-2013_05