Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Ketoisophorone | HCID 62374 | — |
| Edukt | 4-Hydroxy-2,3,6-trimethylphenyl acetate | HCID 119024 | — |
| Edukt | 4-Acetoxy-2,3,6-trimethylphenol | HCID 11019728 | — |
| Edukt | Acetic acid;2,3,5-trimethylbenzene-1,4-diol | HCID 85990707 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | Trimethylhydroquinone | HCID 12785 | 90% |
Reaktionsschritte
To a 500 ml flask was fed 10.0 g of reactant mixture containing 8.64% of trimethylhydroquinone diacetate, 6.24% of a mixture of 4-acetoxy-2,3,6-trimethylphenol and 4-acetoxy-2,3,5-trimethylphenol, and 75.7% of 4-oxoisophorone, and the flask was displaced with nitrogen. Then, 50.0 g of water, 1.0 g of 97% sulfuric acid and 11.3 g of acetic acid were added to the above reactants and they were stirred at 100° C. for 2 hours under atmospheric pressure. The reaction mixture was cooled to a room temperature and 30 ml of hexane was added. The deposited crystals were filtered off to obtain 0.941 g of trimethylhydroquinone at a yield of 90.0%. The purity of these crystals was 100% according to the gas chromatographic analysis. With the retention time in gas chromatography and the identification with a standard sample by the results of IR absorption and MS analysis, it was confirmed that the crystals were trimethylhydroquinone.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06441249B2 |
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| Quelldatensatz | uspto-grants-2002_08 |
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| ORD ID | ord-a6f8b26b5dbe4e72bac7826b517a379f |
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| Quellennotiz | uspto-grants-2002_08 |
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