HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → tert-Butyl 3-(2-iodoethyl)azetidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Tert-butyl 3-(1-hydroxyethyl)azetidine-1-carboxylate | HCID 58348207 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | tert-Butyl 3-(2-iodoethyl)azetidine-1-carboxylate | HCID 19034125 | 83.7% |
Reaction Steps
A stirred solution of 133 (0.78 g, 3.8 mmol), PPh3 (1.1 g, 4.3 mmol), imidazole (0.40 g, 5.8 mmol), and CH3CN (20 mL) at 0° C. was treated with iodine (1.0 g, 4.3 mmol). After 15 min the cooling bath was removed and stirring continued for 5 h. The reaction mixture was then diluted with H2O and extracted with hexanes (5×25 mL then 4×50 mL). The combined extracts were dried (MgSO4) and concentrated. Flash chromatography (silica, 20% EtOAc/hexanes) gave 134 (0.99 g) as a colorless oil. Rf 0.44 (silica, 20% EtOAc/hexanes).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05455243 |
| Source dataset | uspto-grants-1995_10 |
| ORD ID | ord-e1e0715dae7843b69d0127031684e884 |
| Source note | uspto-grants-1995_10 |