HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 59260090, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 59260092 | HCID 59260092 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 59260090 | HCID 59260090 | — |
Reaction Steps
A solution of (2-(4-iodophenyl)-1-methyl-1H-imidazol-4-yl)methanol prepared above (46 mg, 0.15 mmol) in SOCl2 (2 mL) was stirred at room temperature for 15 min. It was concentrated in vacuo to give a residue, which was then partitioned between EtOAc and 5% aq. NaHCO3. The organic phase was separated, dried over Na2SO4, concentrated in vacuo. The residue was dissolved in DMF (2 mL). To the solution, NaN3 (70 mg, 1.1 mmol) was added. After the mixture was stirred at room temperature for 2 days, water and EtOAc were added. The organic layer was separated, dried over Na2SO4, concentrated in vacuo to give (2-(4-iodophenyl)-1-methyl-1H-imidazol-4-yl)methyl azide (46 mg). MS 340.0 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07696352B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-6fe75c46573c4c85b0a4a98b965a20bf |
| Source note | uspto-grants-2010_04 |