Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Chlorobenzene | HCID 7964 | — |
| Edukt | Phenylacetylene | HCID 10821 | — |
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Katalysator | Nickel(II) acetylacetonate | HCID 9834912 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | Phenylacetylene | HCID 10821 | — |
| Produkt | 1,2-Diethynylbenzene | HCID 140862 | — |
Reaktionsschritte
A copolymer prepolymer of diethynylbenzene and phenylacetylene was prepared in refluxing benzene solvent. The polymerization vessel was charged with 60 parts of a 90:10 mixture of m- and p-diethynylbenzenes, 60 parts of phenylacetylene, 600 parts of benzene and 2 parts of chlorobenzene. After heating to reflux, 5 parts of a catalyst solution prepared by adding 0.3 part of nickel acetylacetonate and 0.6 part of triphenylphosphine in 15 parts benzene were added. After 2 hours, an additional 10 parts of this catalyst solution was added. After 5 hours, gas-liquid chromatographic analysis showed that 74% of the diethynylbenzenes and 35% of the phenylacetylene had been converted to copolymer. The copolymer was precipitated by adding the solution to five times its volume of petroleum ether, 26 parts being recovered. This product had a number average molecular weight of about 3,000, an acetylene content of 8.9%, and an aromatic to olefin proton ratio of 5.5:1.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04097460 |
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| Quelldatensatz | uspto-grants-1978_06 |
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| ORD ID | ord-b21e28e6866d411dbc59459847c4c688 |
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| Quellennotiz | uspto-grants-1978_06 |
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