Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Iodoethane | HCID 6340 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 3-Hydroxy-4,5-Dimethoxybenzoic Acid | HCID 74709 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 3,4-Dimethoxy-5-ethoxybenzoic Acid | HCID 18464538 | — |
Reaktionsschritte
Combine 3,4-dimethoxy-5-hydroxybenzoic acid (1.0 g, 5.0 mmol), potassium carbonate (4.2 g, 30.2 mmol), and ethyl iodide (3.9 g, 25.2 mmol) in acetone (50 mL). Heat to reflux. After 24 hours, cool, add methanol (25 mL) and water (5 mL) After 18 hours, concentrate in vacuo to give a residue. Combine the residue and ethanol (50 mL) and potassium hydroxide (0.56 g, 10 mmol). After 18 hours, concentrate in vacuo to give a residue. Partition the residue between ethyl acetate and a 1 M aqueous solution of hydrochloric acid. Extract the aqueous layer three times with ethyl acetate. Combine the organic layers, dry over Na2SO4, filter, and concentrate in vacuo to give a residue. Triturate the residue to give a solid. Collect the solid to give the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06194406B1 |
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| Quelldatensatz | uspto-grants-2001_02 |
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| ORD ID | ord-14ee4b956aae438380ca7ec1d38d4cd2 |
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| Quellennotiz | uspto-grants-2001_02 |
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