HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 2-(4-Bromophenyl)-2-methylpropanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 2-(4-bromophenyl)-2-methylpropanoate | HCID 11277257 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(4-Bromophenyl)-2-methylpropanoic acid | HCID 10933679 | 77.3% |
Reaction Steps
A 100 mL round-bottom flask was charged with ethyl 2-(4-bromophenyl)-2-methylpropanoate (0.670 g, 2.47 mmol) in 2.5 mL of MeOH. Potassium hydroxide (2.0 M, 2.47 mL, 4.94 mmol) was added at 0° C. The reaction was heated to reflux for 2 h. After cooling the reaction was extracted with ethyl acetate. The aqueous layer was acidified with 2M HCl and extracted with dichloromethane (3×). The combined organic layers were dried over sodium sulfate, filtered and concentrated to give 464 mg of 2-(4-bromophenyl)-2-methylpropanoic acid as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07759337B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-ca1931ac95094066853a929a7421d630 |
| Source note | uspto-grants-2010_07 |