HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 218198, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Imidazole, 1,5-dimethyl-2-nitro- | HCID 78888 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 218198 | HCID 218198 | 16% |
Reaction Steps
A mixture of 7.2 g. of 1,5-dimethyl-2-nitroimidazole, 41.2 ml. of benzaldehyde and 7.9 g. of potassium tert-butoxide in 300 ml. of ethanol is refluxed for 35 minutes under nitrogen. The residue, which is obtained by evaporation of the reaction mixture under vacuum, is extracted with ethyl ether and filtered. The ethyl ether solution after concentration yields an oily residue which is chromatographed through 300 g. of silica gel by eluting with chloroform. After evaporation of the solvent under vacuum at 40° C., an oily residue is obtained which crystallizes on standing. After washing with a small amount of methyl ethyl ketone, 1.9 g. (16%) of a product which melts at 170°-180° C. is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03954789 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-bfe9f7e845df498097ac0436c398ff54 |
| Source note | uspto-grants-1976_05 |