Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Naphthalene | HCID 931 | — |
| Edukt | Propylene | HCID 8252 | — |
| Katalysator | Phosphoric Acid | HCID 1004 | — |
| Produkt | 1-(1-Methylethyl)naphthalene | HCID 22535 | — |
Reaktionsschritte
These and other objects and advantages of the invention by the instant process comprises (1) alkylating naphthalene with propylene in the presence of a phosphoric acid catalyst supported on SiO2, at a temperature of 150°-280° C. and a pressure of 5-30 atm. using a mol ratio of 1/5 to 1/20 mol propylene per 1 mol of starting naphthalene, until in the reaction 45 to 65% of the naphthalene has been isopropylated and then without separating off the unreacted naphthalene, (2) further treating the alkylation mixture by heating it in the presence of a phosphoric acid catalyst supported on SiO2 under an inert gas pressure of 5 to 30 atm. to a temperature of 180° to 280° C. until substantially no more β-isopropylnaphthalene is formed from the α-isopropylnaphthalene. There is thereby obtained an isomeric mixture consisting of 90-95% of the β-isopropylnaphthalene isomer. Pure β-isopropylnaphthalene can be recovered from this isomeric reaction product by distillation and crystallization.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04440957 |
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| Quelldatensatz | uspto-grants-1984_04 |
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| ORD ID | ord-3177add7b7ef409285e22e8220f615f3 |
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| Quellennotiz | uspto-grants-1984_04 |
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