HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 3-(2-Bromophenyl)butanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 3-(2-bromophenyl)-3-methylpropionate | HCID 21217383 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(2-Bromophenyl)butanoic acid | HCID 21217379 | 105.5% |
Reaction Steps
To a solution of 28.04 g of ethyl 3-(2-bromophenyl)-3-methylpropionate (109.1 mmole) in ethanol (200 ml) and water (100 ml) was added 12.2 g of potassium hydroxide (218.2 mmole), and the mixture was heated under reflux for 5 hours. After the mixture was left standing at room temperature, it was concentrated to a half of the volume by distillation and diluted again with dilute hydrochloric acid. Dichloromethane was then added, and an aqueous ammonium chloride solution was added before extraction. The organic layer was dried over magnesium sulfate, and the solvent was removed by distillation to give 27.97 g of 3-(2-bromophenyl)-3-methylpropionic acid (quantitatively).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05942459 |
| Source dataset | uspto-grants-1999_08 |
| ORD ID | ord-0ff46ffac2a94c92a1c413651685f292 |
| Source note | uspto-grants-1999_08 |