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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357913Generated: October 30, 2026

Acetone → Tert-butyl 4-(iodomethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1357913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium IodideHCID 5238—
Reactant1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 4184869—
ProductTert-butyl 4-(iodomethyl)piperidine-1-carboxylateHCID 10448961—

Reaction Steps

A mixture of 1-(t-butoxycarbonyl)piperidin-4-yl methanesulfonate (13.58 g, 46.4 mmol) and sodium iodide (34.68 g, 232 mmol) in acetone (80 mL) was heated to reflux for 3 h. The mixture was partitioned between ether (350 mL) and water (350 mL). The organic layer was washed with saturated aq. brine (250 mL), and the aqueous layers were extracted in succession with ether (250 mL). The combined organic layers were dried (sodium sulfate), decanted, and evaporated to give the title compound (14.8 g) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06593346B2
Source datasetuspto-grants-2003_07
ORD IDord-dfb0d2ae378c430eab1e83f2f877d989
Source noteuspto-grants-2003_07