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HRID 27145Erstellt: 24. Oktober 2026
1-Butanol → 1-(N-benzyloxycarbonyl-p-toluidinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride
https://huagongshe.com/de/reaction/27145
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1-Butanol | HCID 263 | — |
| Edukt | Dopamine Hydrochloride | HCID 65340 | — |
| Edukt | N-benzyloxycarbonyl-p-toluidinoacetaldehyde diethyl acetal | HCID 20460580 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1-(N-benzyloxycarbonyl-p-toluidinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride | HCID 20460590 | 63,4% |
Reaktionsschritte
N-benzyloxycarbonyl-p-toluidinoacetaldehyde 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) and then the mixture was refluxed for 9.5 hours in a stream of nitrogen. In the course of the reaction, the above-mentioned acetal (0.6 g) was twice added to the mixture, after 5 hours and after 7.5 hours from the beginning of the reaction. The reaction mixture was concentrated and the residue was washed with ether and dissolved in hot water (300 ml). After the insoluble material was filtered off, the filtrate was washed with ethyl acetate and treated with activated charcoal. The aqueous layer was concentrated to dryness to give amorphous 1-(N-benzyloxycarbonyl-p-toluidinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride (3.8 g), mp 125° 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-450ae31ddfe24a7bb4c2f7e67aba0817 |
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| Quellennotiz | uspto-grants-1980_09 |
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