HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7084Erstellt: 23. Oktober 2026
Benzaldehyde → 4-hydroxy-3-methoxy-N-[1-oxo-2-phenylmethylidene-1,2,3,4-tetrahydronaphthalen-7-yl]phenylacetamide
https://huagongshe.com/de/reaction/7084
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzaldehyde | HCID 240 | — |
| Edukt | 7-Amino-1,2,3,4-tetrahydronaphthalen-1-one | HCID 327177 | — |
| Edukt | 3-(Cyclohexen-1-yl)aniline | HCID 6709749 | — |
| Edukt | 4-hydroxy-3-methoxy-N-[1-oxo-1,2,3,4-tetrahydronaphthalen-7-yl]phenylacetamide | HCID 22019659 | — |
| Lösungsmittel | Ethanol hydrochloride | HCID 21887872 | — |
| Produkt | 4-hydroxy-3-methoxy-N-[1-oxo-2-phenylmethylidene-1,2,3,4-tetrahydronaphthalen-7-yl]phenylacetamide | HCID 69663967 | — |
Reaktionsschritte
Instead of 3-(cyclohexen-1-yl)aniline (Intermediate 2) in Example 9, 7-amino-1-tetralone is treated in a similar manner to Example 9. The resulting 4-hydroxy-3-methoxy-N-[1-oxo-1,2,3,4-tetrahydronaphthalen-7-yl]phenylacetamide (1 g) is dissolved in 30% hydrogen chloride-ethanol (5 ml), and thereto is added benzaldehyde (433 mg). The mixture is stirred at 25° C. for 18 hours. The precipitated crystals are collected by filtration, and washed with diethyl ether to give the desired compound (700 mg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07084176B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-18b1747dcc8a42479959da4aec8199c0 |
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| Quellennotiz | uspto-grants-2006_08 |
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