HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262613Generated: October 29, 2026
Imidazole → Tert-butyl 3-iodoazetidine-1-carboxylate
https://huagongshe.com/reaction/2262613
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Tert-butyl 3-hydroxyazetidine-1-carboxylate | HCID 2756801 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Tert-butyl 3-iodoazetidine-1-carboxylate | HCID 11000522 | 95% |
Reaction Steps
A solution of 3-hydroxy-azetidine-1-carboxylic acid tert-butyl ester (3.35 g, 19.34 mmol) in toluene (200 ml) was treated with imidazole (3.95 g, 58.01 mmol), triphenylphosphine (10.14 g, 38.65 mmol) and I2 (7.36 g, 28.99 mmol). The mixture was heated at 100° C. for 1 h, cooled down to room temperature and next poured into saturated aqueous NaHCO3 (30 ml). Excess triphenylphosphine was destroyed by addition of iodine until I2 coloration persisted in organic layer. The latter was washed with 5% aqueous Na2S2O3, dried over Na2SO4 and evaporated. Purification of the crude product by flash column chromatography (heptane:ethyl acetate, 2:1) provides the title compound (5.19 g, 95%) as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07851463B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-ffdbad68405a45af8939b193f824dd85 |
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| Source note | uspto-grants-2010_12 |
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