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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207852Generated: November 1, 2026

Imidazole → Benzyl 4-iodopiperidine-1-carboxylate

https://huagongshe.com/reaction/2207852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
ReactantBenzyl 4-Hydroxy-1-piperidinecarboxylateHCID 2794620—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl 4-iodopiperidine-1-carboxylateHCID 5324982642%

Reaction Steps

Iodine (17.6 g, 69.2 mmol) was added dropwise as a solution in THF (40 mL) over 1 hour to an ice cold solution of benzyl 4-hydroxypiperidine-1-carboxylate (15.5 g, 65.9 mmol), imidazole (4.71 g, 69.2 mmol), and triphenylphosphine (18.2 g, 69.2 mmol) in THF (40 mL). This resulting red solution was stirred overnight with warming to room temperature, then cooled back to 0° C. before being quenched with 10% aqueous sodium sulfite. The resulting biphasic mixture was separated and the aqueous layer was extracted with ethyl acetate (1×). The combined extracts were dried over magnesium sulfate (MgSO4), filtered, and concentrated in vacuo to give an oil that was purified by silica gel chromatography (10% EtOAc/hexane) to give benzyl 4-iodopiperidine-1-carboxylate as a coloreless oil (9.50 g, 42% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376450B2
Source datasetuspto-grants-2016_06
ORD IDord-63edbce632404acca316989b42a506e9
Source noteuspto-grants-2016_06