HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454954Generated: November 1, 2026
Imidazole → Benzyl 4-iodopiperidine-1-carboxylate
https://huagongshe.com/reaction/454954
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Benzyl 4-Hydroxy-1-piperidinecarboxylate | HCID 2794620 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzyl 4-iodopiperidine-1-carboxylate | HCID 53249826 | 42% |
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 colorless oil (9.50 g, 42% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08497265B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-2ea87fc4e3904c5db847e3dba916679c |
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| Source note | uspto-grants-2013_07 |
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