HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 21273214, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | N,N-Dimethylacrylamide | HCID 17587 | — |
| Reactant | HCID 21273227 | HCID 21273227 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 21273214 | HCID 21273214 | 90% |
Reaction Steps
A mixture of 4-iodo-2-methyl-1-(4-methylbenzenesulphonyl)-1H-imidazole (3.62 g), N,N-dimethylacrylamide (1.05 g), palladium (II) acetate (125 mg) and triethylamine (2 ml) in acetonitrile (3 ml) was heated at 120° under nitrogen for 2.5 h. The cooled mixture waspartitioned between chloroform (3×50 ml) and 2N sodium carbonate (75 ml), and the combined organic layers were dried and evaporated in vacuo to leave a solid (ca. 3.0 g). This solid was purified by FCC eluting with chloroform to give the crystalline title compound (1.55 g), m.p. 162°-163°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04808581 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-b6d7b17606094541a79e7b5ae969ca95 |
| Source note | uspto-grants-1989_02 |