Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,3-Butadiene | HCID 7845 | — |
| Edukt | 2-Methoxyethanol | HCID 8019 | — |
| Edukt | 5-Nitronaphthalene-1,4-dione | HCID 12336402 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 5-Nitro-1,4,4a,9a-tetrahydroanthraquinone | HCID 10868940 | 94% |
Reaktionsschritte
A mixture comprising 10 g of the obtained 5-nitro-1,4-naphthoquinone, 3.3 g of 1,3-butadiene and 40 ml of ethylene glycol monomethyl ether was retained in a 100-milliliter autoclave at 50° C. for 6 hours with stirring. The reaction pressure was initially 1.2 atmospheres and 1.0 atmosphere when the reaction was over. Thereafter, 60 ml of water was added to the reaction mixture and cooled to 25° C. The precipitated crystals were filtered, washed with 30 ml of methyl alcohol and dried under reduced pressure to obtain 11.9 g of white 5-nitro-1,4,4a,9a-tetrahydroanthraquinone having a purity of 98%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05213665 |
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| Quelldatensatz | uspto-grants-1993_05 |
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| ORD ID | ord-98389420ba7b4482934597b289074689 |
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| Quellennotiz | uspto-grants-1993_05 |
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