Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Citric Acid | HCID 311 | — |
| Edukt | 3,4-Dimethoxytoluene | HCID 68126 | — |
| Edukt | Monobasic potassium phosphate | HCID 516951 | — |
| Edukt | 6-benzothiazolesulfonic acid, 2,2'-azinobis(3-ethyl-2,3-dihydro-, diammonium salt | HCID 9570474 | — |
| Edukt | Dipotassium hydrogen phosphate citric acid | HCID 21698641 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Veratryl alcohol | HCID 7118 | — |
| Produkt | Veratraldehyde | HCID 8419 | — |
Reaktionsschritte
22 ml of a dipotassium hydrogen phosphate/citric acid buffer solution of pH 4.5 (prepared by titrating a 0.2 M potassium dihydrogen phosphate solution with a 0.1 M citric acid solution and diluting to 1/4) were treated at 45° C. with 243 mg (1.60 mmol) of 3,4-dimethoxytoluene in 1 ml of ethanol. 0.180 mmol of a mediator (Table 1) was added with stirring. After approx. 10 minutes, the mixture was treated with 5 ml of an aqueous solution of 2 mg/ml laccase from Trametes versicolor (specific activity: approx. 18 IU/mg, defined with ABTS as substrate). After a reaction time of 22 hours with exposure to air, the reaction solution was extracted with chloroform and examined by N spectroscopy and gas chromatography. Yields of 3,4-dimethoxybenzaldehyde and 3,4-dimethoxybenzyl alcohol, see Table 1.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06023000 |
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| Quelldatensatz | uspto-grants-2000_02 |
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| ORD ID | ord-15dd6d7afc2847339f67aa9bf42f1109 |
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| Quellennotiz | uspto-grants-2000_02 |
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