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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 1-Tert-butyl 4-chloromethyl piperidine-1,4-dicarboxylate | HCID 10107566 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Iodomethyl n-tert-butoxycarbonyl-4-piperidylcarboxylate | HCID 59443277 | 94% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129375B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-8b69c013dcb64092897ef7e0a9f254f4 |
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| Source note | uspto-grants-2012_03 |
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