HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → Ethyl p-[5-(1-imidazolyl)pentyloxy]phenoxyacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-{[5-(1H-Imidazol-1-yl)pentyl]oxy}phenol | HCID 13219140 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl p-[5-(1-imidazolyl)pentyloxy]phenoxyacetate | HCID 14327317 | — |
Reaction Steps
To a solution of 2.46 g p-[5-(1-imidazolyl)pentyloxy]phenol and 1.2 ml ethyl bromoacetate in 25 ml anhydrous N,N-dimethylformamide, was added under ice cooling and with stirring 440 mg of 60% sodium hydride in oil, and stirring was continued at room temperature for ten minutes. The solvent was distilled off, the residue was dissolved in chloroform, and the solution was washed with water and dried over anhydrous sodium sulfate. After distilling off, the chloroform, the residue was purified by silical gel column chromatography, affording 2.7 g of ethyl p-[5-(1-imidazolyl)pentyloxy]phenoxyacetate as oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04987147 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-69e8f2b20e2f42b594b8a696e47a8d02 |
| Source note | uspto-grants-1991_01 |