Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethanol | HCID 702 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | 3-Phenoxyphenylacetic acid | HCID 141749 | — |
| Produkt | Ethyl (3-phenoxyphenyl)acetate | HCID 12509092 | — |
Reaktionsschritte
(3-Phenoxyphenyl)acetic acid (11.5 g) and 36N aqueous sulphuric acid solution (3 cc) in ethanol (200 cc) are brought to boiling for 72 hours. After being cooled to approximately 20° C., the reaction mixture is concentrated to dryness at 50° C. under reduced pressure (20 mm Hg; 2.7 kPa). The oil is dissolved in dichloromethane (300 cc); the organic phase is washed with water (150 cc), dried over anhydrous magnesium sulphate, filtered and concentrated to dryness at 40° C. under reduced pressure (20 mm Hg; 2.7 kPa). The residue is dissolved in a mixture (20 cc) of cyclohexane and ethyl acetate (50:50 by volume), and the solution is poured onto silica (400 g) contained in a column 5 cm in diameter. Elution is performed with a mixture of cyclohexane and ethyl acetate (50:50 by volume), and the corresponding eluate is concentrated to dryness at 40° C. under reduced pressure (20 mm Hg; 2.7 kPa). Ethyl (3-phenoxyphenyl)acetate (7.4 g) is thereby obtained, and is used in the crude state in the subsequent syntheses.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04886835 |
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| Quelldatensatz | uspto-grants-1989_12 |
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| ORD ID | ord-70ed4016b51a42b78a92452f147dcbd8 |
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| Quellennotiz | uspto-grants-1989_12 |
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