HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → [4-(Trifluoromethyl)-1H-imidazol-1-yl]acetic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 178418921 | HCID 178418921 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | [4-(Trifluoromethyl)-1H-imidazol-1-yl]acetic acid ethyl ester | HCID 59603647 | — |
Reaction Steps
2.0 g (14.7 mmol) 4-(trifluoromethyl)-1H-imidazole are initially introduced into 5.5 ml (4.7 g, 14.7 mmol) 21% strength sodium ethylate solution in ethanol and 1.8 ml (2.7 g, 16.2 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. The product is obtained as a 9:1 mixture of the two regioisomers and is further reacted as such.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08987261B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-6ff10ab8616d4f208a376441ebf097e7 |
| Source note | uspto-grants-2015_03 |