HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Acetate → ethyl 4-amino-2-butyl-1H-imidazole-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 6917117 | HCID 6917117 | — |
| Reactant | HCID 86746837 | HCID 86746837 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | ethyl 4-amino-2-butyl-1H-imidazole-5-carboxylate | HCID 19106923 | 69.7% |
Reaction Steps
A mixture of methyl iminovalerate hydrochloride (4.8 g), ethyl 2-amino-2-cyanoacetate oxalate (4.0 g), anhydrous sodium acetate (9.1 g) and absolute ethanol (75 mL) was stirred at room temperature for 18 hours. Solids were removed by filtration and the filtrate was evaporated. The residue was partitioned between ethyl acetate and water. The ethyl acetate layer was washed with saturated NaCl, dried over MgSO4, and evaporated Flash chromatography on silica gel, eluting with a gradient of dichloromethane-ethyl acetate (75:25) to ethyl acetate gives the title compound (2.7 g) as a pale yellow solid, mp 103°-106° C. MS (DEI) 211 (m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05210211 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-011fd8681cb141dd97b9505d87e4b518 |
| Source note | uspto-grants-1993_05 |