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HRID 27146Erstellt: 24. Oktober 2026
1-Butanol → 1-(N-benzyloxycarbonyl-p-fluoroanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride
https://huagongshe.com/de/reaction/27146
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Butanol | HCID 263 | — |
| Edukt | Dopamine Hydrochloride | HCID 65340 | — |
| Edukt | N-benzyloxycarbonyl-p-fluoroanilinoacetaldehyde diethyl acetal | HCID 20460532 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1-(N-benzyloxycarbonyl-p-fluoroanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride | HCID 20460542 | 44,6% |
Reaktionsschritte
N-benzyloxycarbonyl-p-fluoroanilinoacetaldehyde diethyl acetal (6 g) and 3,4-dihydroxyphenethylamine hydrochloride (2.5 g) were added to a mixture of n-butyl alcohol (60 ml) and water (8.5 ml). The mixture was then refluxed for 11 hours in a stream of nitrogen. In the course of the reaction, amounts of the above-mentioned acetal (0.6 g and 1.2 g) were added to the mixture after 4.5 hours and 6 hours, respectively, from the beginning of the reaction. The reaction mixture was concentrated to dryness and the residue was washed with ether and dissolved in water. The solution was washed with ether and concentrated to dryness to give amorphous 1-(N-benzyloxycarbonyl-p-fluoroanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride (2.7 g), mp 122° C. (dec.).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04220647 |
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| Quelldatensatz | uspto-grants-1980_09 |
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| ORD ID | ord-5ff7cb659ce54ae3ac8a4d37277a9d40 |
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| Quellennotiz | uspto-grants-1980_09 |
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