Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 2-Methyl-2-butene | HCID 10553 | — |
| Edukt | Methyl 4-formyl-3-methoxybenzoate | HCID 10631650 | — |
| Edukt | Sodium Chlorite | HCID 23668197 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | tert-Butanol | HCID 6386 | — |
| Produkt | 2-Methoxy-4-(methoxycarbonyl)benzoic acid | HCID 59340334 | 47% |
Reaktionsschritte
To a stirred solution of 4-formyl-3-methoxybenzoic acid methyl ester (5.0 g, 26 mmol; prepared as described in Preparation 17) in tert-butyl alcohol (200 mL) was added NaH2PO4-2H2O (3.6 g, 26 mmol), water (50 mL), 2-methyl-2-butene (11 mL, 104 mmol), and finally NaClO2 (7.02 g, 78 mmol). The reaction was allowed to stir at room temperature for 4 hours. The solvent was then removed under reduced pressure. The crude reaction mixture was then dissolved in DCM (200 mL) and the product was extracted with 1N NaOH (200 mL). The aqueous layer was washed with DCM (200 mL) and then neutralized with 6N HCl (˜40 mL) and the product extracted with DCM (200 mL). The organic layer was then washed with water (100 mL), NaCl (sat.) (100 mL), dried over MgSO4 and then filtered. The solvent was removed under reduced pressure. The crude material was sufficiently pure to use without further purification. The title intermediate was obtained in 47% yield (2.4 g, 12.3 mmol).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07728144B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-b320caf1293a42f1b79feab23a43166c |
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| Quellennotiz | uspto-grants-2010_06 |
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