HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348414Generated: November 1, 2026
Potassium Iodide → Tert-butyl 3-iodoazetidine-1-carboxylate
https://huagongshe.com/reaction/348414
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Tert-butyl 3-(methanesulfonyloxy)azetidine-1-carboxylate | HCID 10753243 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl 3-iodoazetidine-1-carboxylate | HCID 11000522 | — |
Reaction Steps
A mixture of tert-butyl 3-[(methylsulphonyl)oxy]-1-azetidinecarboxylate (Synlett; 1998; 379), (5.0 g, 19.9 mmol), and potassium iodide (16.5 g, 99.4 mmol) in N,N-dimethylformamide (25 ml), was heated at 100° C. for 42 hours. The cooled mixture was partitioned between water and ethyl acetate, and the layers separated. The organic phase was dried (MgSO4), concentrated under reduced pressure and the residue azeotroped with xylene. The crude product was purified by column chromatography on silica gel using dichloromethane as eluant, to give the title compound, 3.26 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07176311B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-2e629d92b8ac4abb96244ce52487c413 |
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| Source note | uspto-grants-2007_02 |
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