HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetoacetate → Diethyl 4-[4-(1H-imidazol-1-yl)phenyl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 4-(1H-imidazol-1-yl)benzaldehyde | HCID 736530 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Diethyl 4-[4-(1H-imidazol-1-yl)phenyl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate | HCID 10475789 | 65% |
Reaction Steps
A mixture of 17.2 g (0.1 mol) of 4-(1H-imidazol-1-yl)benzaldehyde, 26 g (0.2 mol) of ethyl acetoacetate and 5 ml of concentrated NH4OH in absolute ethanol (25 ml) was refluxed for 6 hours. The mixture was poured into 500 ml of ice-water and the aqueous solution was extracted with methylene chloride. The organic layers were put together, dried over CaCl2 and evaporated under vacuum. The crude product was recrystallized from Et2O, giving 25.7 g (65%) of 1,4-dihydro-2,6-dimethyl-4-[4-(1H-imidazol-1-yl)phenyl]-3,5-pyridinedicarboxylic acid, diethyl ester, m.p. 231°-233° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05362729 |
| Source dataset | uspto-grants-1994_11 |
| ORD ID | ord-30c38d9714954b91b75fb3cf10a5e076 |
| Source note | uspto-grants-1994_11 |