HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 3-(2-Bromophenyl)butanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 3-(2-bromophenyl)-3-methylpropionate | HCID 21217383 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(2-Bromophenyl)butanoic acid | HCID 21217379 | 105.5% |
Reaction Steps
To a solution of ethyl 3-(2-bromophenyl)-3-methylpropionate (28.04 g, 109.1 mmole) in the mixture of ethanol (200 ml) and water (100 ml) was added potassium hydroxide (12.2 g, 218.2 mmole). The solution was heated under reflux for 5 hours, left standing overnight as it was, the solvent was removed to about half of its original amount, and dilute hydrochloric acid was added to the concentrate. To this mixture was added dichloromethane followed by an aqueous ammonium chloride solution, the layers were separated, and the organic layer was dried over magnesium sulfate. The solvent was removed by distillation under reduced pressure to give 3-(2-bromophenyl)-3-methylpropionic acid (27.97 g, quant.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05594081 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-1d5978a6178c4c8380f56f12d2549544 |
| Source note | uspto-grants-1997_01 |