Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2,3-Dimethoxybenzaldehyde | HCID 66581 | — |
| Edukt | 2-Amino-1-(3,4-dimethoxyphenyl)ethan-1-ol hydrochloride | HCID 12888909 | — |
| Edukt | HCID 178418435 | HCID 178418435 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | Veratryl alcohol | HCID 7118 | — |
Reaktionsschritte
1.0 g of α-(aminomethyl)-3,4-dimethoxybenzyl alcohol hydrochloride was suspended in 5 ml of methanol, and after adding thereto 0.85 g of 2,3-dimethoxybenzaldehyde, 0.63 ml of triethylamine was added dropwise to the mixture while stirring at room temperature. The mixture was heated under reflux for 30 minutes, and 0.24 g of sodium boron hydride was added slowly to the mixture while stirring under ice cooling. After the foaming stopped, the mixture was concentrated. The residue was subjected to a separating procedure with chloroform and water, the chloroform layer was collected, washed with water, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was recrystallized from ethyl acetate-n-hexane, giving 1.07 g of α-[[2,3-dimethoxybenzyl)amino]methyl]-3,4-dimethoxybenzyl alcohol, m.p. 96°-97° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05623074 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-3bcdb4656b234fc0b193760fcf8acf5b |
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| Quellennotiz | uspto-grants-1997_04 |
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