HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-ethyl-4-methyl-1H-imidazole-5-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | 5-Methyl-1H-imidazole-4-carbaldehyde | HCID 2795887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-ethyl-4-methyl-1H-imidazole-5-carbaldehyde | HCID 59589463 | 13% |
Reaction Steps
To 4-methyl-1H-imidazole-5-carbaldehyde (5.0 g, 45.4 mmol) in anhydrous THF (50 mL) was added diaza(1,3)bicyclo[5.4.0]undecane (DBU, 6.8 mL, 45.4 mmol), and iodoethane (3.4 mL, 45.4 mmol). The mixture was stirred at room temperature overnight. Water (50 mL) was added before the THF was evaporated. The mixture was extracted with EtOAc (1×50 mL) and 2-butanol (2×50 mL). The organic extracts were combined, dried over MgSO4, filtered, evaporated, and dried in vacuo. The crude product was purified by flash chromatography (0-1% MeOH/DCM), affording 1-ethyl-4-methyl-1H-imidazole-5-carbaldehyde (806 mg, 13% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09315521B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-c62358bd86e34960842cc448a873fb72 |
| Source note | uspto-grants-2016_04 |