HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → ethyl 2-(4-cyano-1H-imidazol-1-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 178510437 | HCID 178510437 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | ethyl 2-(4-cyano-1H-imidazol-1-yl)acetate | HCID 68753735 | — |
Reaction Steps
3.3 g (35.3 mmol) 1H-imidazole-4-carbonitrile [Matthews et al., J. Org. Chem. 1986, 51, 3228-3231] are initially introduced into 13.2 ml (11.5 g, 35.3 mmol) 21% strength sodium ethylate solution in ethanol and 4.3 ml (6.5 g, 38.9 mmol) ethyl bromoacetate are added. The reaction mixture is stirred at RT for 16 h. For working up, the solid which has precipitated out is filtered off, the residue on the filter is washed with ethanol and the filtrate is concentrated in vacuo. Diisopropyl ether is added to the residue, the mixture is filtered again, the filtrate is concentrated again on a rotary evaporator and the residue is dried in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08653111B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-cf7ef924dc23455a9eb63ec62f4e3ee7 |
| Source note | uspto-grants-2014_02 |