Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetralin | HCID 8404 | — |
| Reactant | Dodecanedioic Acid | HCID 12736 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 20399698 | HCID 20399698 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | Naphthalene | HCID 931 | — |
Reaction Steps
The procedure of Example 1 was repeated using 70 g (304 mmols) of dodecanedioic acid 13.2 g (100 mmols) of tetralin, 0.16 g (0.71 mmols) of Pd(OAc)2, 0.42 g (1.42 mmols) of Sb(OAc)3, 0.07 g (0.71 mmols) of KOAc and 5 ml heptane. Reaction mixture was heated and the temperature of the reaction was maintained at 178±2° C. Oxygen was bubbled continuously at a rate of 200 cc/min. Reaction was carried out for 3 hrs. during which time the water produced was removed azeotropically with heptane. Reaction mixture was analyzed by GLC which showed the formation of 3.65% (by wt.) naphthyl dodecanedioate. Only a trace of naphthalene formed in the reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04512927 |
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| Source dataset | uspto-grants-1985_04 |
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| ORD ID | ord-e1e0b19b4d2d49ddae1313efb81b5f71 |
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| Source note | uspto-grants-1985_04 |
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