HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-(2-Fluorophenyl)-2-methylpropanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methyl 2-(2-fluorophenyl)-2-methylpropanoate | HCID 57421199 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-Fluorophenyl)-2-methylpropanoic acid | HCID 25916725 | 81.3% |
Reaction Conditions
| Temperature | 130 °C |
|---|
Reaction Steps
A flask containing a solution of methyl 2-(2-fluorophenyl)-2-methylpropanoate (5.2 g, 27 mmol), KOH (2.9 mL, 106 mmol), water (20.0 mL), and EtOH (100 mL) was sealed and heated at 130° C. for 2 hours. Removal of solvent in vacuo provided a yellow oil that was diluted with water. The aqueous mixture was extracted with DCM (1×100 mL), and the organic layer was separated. The aqueous layer was acidified to a pH of 1 with 5N HCl and then extracted with EtOAc (2×100 mL). The organic layers were dried (Na2SO4), filtered, and concentrated in vacuo to afford 4 g of the product as a solid. MS (m/z)=181 (M−1)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07635715B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-ac6cb7977342438ebc576b3370084ace |
| Source note | uspto-grants-2009_12 |