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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091343Generated: October 25, 2026

Sodium Iodide → Iodomethyl n-tert-butoxycarbonyl-4-piperidylcarboxylate

https://huagongshe.com/reaction/1091343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant1-Tert-butyl 4-chloromethyl piperidine-1,4-dicarboxylateHCID 10107566—
SolventAcetonitrileHCID 6342—
ProductIodomethyl n-tert-butoxycarbonyl-4-piperidylcarboxylateHCID 5944327794%

Reaction Steps

To a solution of NaI (1.6 g, 11.09 mmol) in dry acetonitrile (8 mL) was added dropwise 1-tert-butyl 4-chloromethyl piperidine-1,4-dicarboxylate (2.8 g, 10.08 mmol) in 2 mL of acetonitrile. The mixture turned dark orange and was stirred at rt in the dark for 24 h. The reaction mixture was filtered to remove NaCl and the filtrate was concentrated in vacuo. The remaining residue was partitioned between DCM and 5% aq NaHSO3 solution. The organic layer was washed with water and brine, dried (Na2SO4), and concentrated in vacuo to give 1-tert-butyl 4-iodomethyl piperidine-1,4-dicarboxylate as a pale yellow oil (3.5 g, 94%). Attempts to characterize by NMR in DMSO-d6 resulted in rapid decomposition. The material was stored in the dark at −20° C. to minimize decomposition before further use. LCMS: MH=370.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129375B2
Source datasetuspto-grants-2012_03
ORD IDord-8b69c013dcb64092897ef7e0a9f254f4
Source noteuspto-grants-2012_03