HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 13961199, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | HCID 13961197 | HCID 13961197 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 13961199 | HCID 13961199 | — |
Reaction Steps
20.9 g (0.66 mol) of ethyl 4-amino-3-(2-chlorobenzoyl)-phenylacetate are dissolved in 170 ml of anhydrous dioxane. First 5.2 ml of absolute pyridine are added and then 13.3 g (0.066 mol) of bromoacetylbromide are added dropwise at room temperature and the mixture is stirred for 24 hours. The suspension is filtered through Kieselgur. The Kieselgur is washed with ether, and the combined filtrates are concentrated in vacuo. The resulting residue is induced to crystallise by addition of ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05116971 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-e1db2ca806d6460a88d9876bbab13ed4 |
| Source note | uspto-grants-1992_05 |