HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → ethyl 2-(1H-imidazol-1-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | ethyl 2-(1H-imidazol-1-yl)acetate | HCID 3798501 | — |
Reaction Steps
118.2 g (5.1 mmol) of sodium are added slowly to 2.5 litres of ethanol. 350.0 g (5.1 mol) of imidazole and 570 ml (858.6 g, 5.1 mol) of ethyl bromoacetate are added dropwise at an internal temperature of 20-25° C. The mixture is stirred at RT for 24 h. The precipitated solid is filtered off, the ethanol is removed under reduced pressure and the mixture is filtered again. The residue is purified by column chromatography on silica gel (mobile phase ethyl acetate). Yield: 639.0 g (81% of theory)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08580778B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-4dc5c349ee824dfcbf97ea2f02f4f5dc |
| Source note | uspto-grants-2013_11 |