Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,3-Butadiene | HCID 7845 | — |
| Edukt | 1,5-Dimethylnaphthalene | HCID 11306 | — |
| Lösungsmittel | O-Xylene | HCID 7237 | — |
| Produkt | 2,6-Dimethylnaphthalene | HCID 11387 | — |
Reaktionsschritte
The present inventors synthesized 1,5-DMN from o-xylene and butadiene as the starting raw materials and isomerized the resultant 1,5-DMN to obtain the mixture of isomers consisting essentially of 1,5-, 1,6- and 2,6-DMNs, which was cooled as it is to precipitate 2,6-DMN crystal in the form of scale. The crystal thus obtained was poor in the efficiency of separation from the mother liquor at the time of filtration, whereby it was difficult to obtain highly pure 2,6-DMN. As is the case with the foregoing, 2,6-DMN crystal in the form of scale was obtained from the mixture of isomers containing 2,7-, 1,7-DMN, etc. other than 1,5-, 1,6- and 2,6-DMN as the starting raw material for crystallization, but it was extremely poor in filtration efficiency.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05948949 |
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| Quelldatensatz | uspto-grants-1999_09 |
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| ORD ID | ord-a4e82ec4219f4f7aa3863c06354f3ddf |
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| Quellennotiz | uspto-grants-1999_09 |
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