Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Hydrogen Peroxide | HCID 784 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 4-(2,2,2-Trifluoroethoxy)benzaldehyde | HCID 4770946 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 4-(2,2,2-Trifluoroethoxy)benzoic acid | HCID 3763901 | 91% |
Reaktionsschritte
To a stirred solution of 50% w/v KOH (1.2 ml) and 4-(2,2,2-trifluoroethoxy)-benzaldehyde (0.6 g, 2.94 mmol) in MeOH (5 ml) at 65° C. was added dropwise over 20 min aqueous hydrogen peroxide (30 wt. % in water, 2.4 ml). On completion of the addition the reaction mixture was heated at 65° C. for a further 10 min. On cooling to room temperature, the reaction mixture was acidified with 1 M HCl and extracted with Et2O (3×30 ml). The combined organic extracts were washed with brine (20 ml), dried (Na2SO4) and the solvent removed under reduced pressure to give the title compound (0.59 g, 91%) as a pale yellow solid which was used without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08895313B2 |
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| Quelldatensatz | uspto-grants-2014_11 |
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| ORD ID | ord-2f2e71168b0443d89330b97e317e4e09 |
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| Quellennotiz | uspto-grants-2014_11 |
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