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HRID 483713Erstellt: 24. Oktober 2026
2,3-Dihydroxybutanedioic Acid → 4-Formylbenzyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl ether
https://huagongshe.com/de/reaction/483713
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2,3-Dihydroxybutanedioic Acid | HCID 875 | — |
| Edukt | Sodium Sulfate | HCID 24436 | — |
| Edukt | 4-Cyanobenzyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl ether | HCID 14850577 | — |
| Edukt | Diisobutylaluminumhydride | HCID 21225700 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 4-Formylbenzyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl ether | HCID 14850579 | — |
Reaktionsschritte
15.5 ml (19.7 mmol) of diisobutylaluminum hydride solution (20% in hexane) were added dropwise under nitrogen to a solution of 3 g (9.4 mmol) of 4-cyanobenzyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl ether in 40 ml of dry ether at 25° C. The mixture was stirred at 25° C. for 40 min and then 250 ml of saturated tartaric acid solution were added dropwise. Subsequently, a little sodium sulfate solution was added, and the phases were separated. The aqueous phase was extracted with ether, and the organic extract was washed with saturated tartaric acid solution and water, dried over Na2SO4 and concentrated. Recrystallization from methanol resulted in 1.4 g of the title compound of melting point 102°-104° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05225601 |
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| Quelldatensatz | uspto-grants-1993_07 |
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| ORD ID | ord-3a18719b85964a5597bd3a8d2ad76551 |
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| Quellennotiz | uspto-grants-1993_07 |
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