HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 5-(azidomethyl)-1H-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178519868 | HCID 178519868 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-(azidomethyl)-1H-imidazole | HCID 178514575 | — |
Reaction Steps
To a suspension of 4-hydroxymethylimidazole II-1 (1.09 g, 11.1 mmol) in CH3CN (12 mL), SOCl2 (5 mL) was added. After being stirred at room temperature for 30 min, the suspension became clear. After stirring for additional 2 h, the solution was concentrated in vacuo to give a solid, which was then dissolved in DMF (15 mL). To the solution, NaN3 (2.16 g, 33.2 mmol) was added. After the mixture was stirred at room temperature overnight, water and EtOAc were added, then 5% aq. NaHCO3 was also added. The organic layer was separated, dried over Na2SO4, concentrated in vacuo to give 4-azidomethylimidazole as a solid (0.759 g). MS 124.1 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07767697B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-1fa0e4e9ba4e485ca1751924d6ea54e4 |
| Source note | uspto-grants-2010_08 |