HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2,2'-[5-(5-Formylimidazol-1-yl)-1,3-phenylene]di(2-methylpropiononitrile)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1-(triphenylmethyl)-1H-imidazole-4-carbaldehyde | HCID 618233 | — |
| Reactant | 2,2'-(5-Bromomethyl-1,3-phenylene)di(2-methylpropiononitrile) | HCID 11522359 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,2'-[5-(5-Formylimidazol-1-yl)-1,3-phenylene]di(2-methylpropiononitrile) | HCID 19349390 | — |
Reaction Steps
A mixture of 4-formyl-1-tritylimidazole (0.5 g), 2,2'-(5-bromomethyl-1,3-phenylene)di(2-methylpropiononitrile) and acetonitrile (2 ml) was heated under reflux for 30 h. The reaction mixture was treated with acetic acid (8 ml) and water (2 ml) and the mixture was then heated at 90° for 1 h. The mixture was diluted with water (20 ml) and washed with ether, the aqueous phase was basified with sodium carbonate, and the mixture was extracted three times with ethyl acetate. The combined extracts were dried and evaporated to dryness, and the residue was purified by flash chromatography using methanol (2% by volume) in chloroform as eluant, to give 2,2'-[5-(5-formylimidazol-1-yl)-1,3-phenylene]di(2-methylpropiononitrile), mp 108°-111°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04935437 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-0556d3de971f4cc28e9e282b3275bd59 |
| Source note | uspto-grants-1990_06 |