Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorobenzene | HCID 7964 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1,4-Diphenyl-1,3-butadiyne | HCID 70174 | — |
| Reactant | 1,2-Diethynylbenzene | HCID 140862 | — |
| Catalyst | Nickel(II) acetylacetonate | HCID 9834912 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1,4-Diphenyl-1,3-butadiyne | HCID 70174 | — |
| Product | 1,4-Diethynylbenzene | HCID 120463 | — |
Reaction Steps
A copolymer prepolymer of diphenylbutadiyne and p-diethynylbenzene was prepared in refluxing benzene solvent. The polymerization vessel was charged with 63 parts of diphenylbutadiyne, 2 parts of diethynylbenzene, 600 parts of benzene, and 2 parts of chlorobenzene. After heating to reflux, 2 parts of a catalyst mixture prepared by mixing 2 parts of nickel acetylacetonate and 4 parts of triphenylphosphine in 20 parts of benzene were added. After 1 hour, an additional 10 parts of diethynylbenzene was added. After 2 hours, 10 parts of diethynylbenzene and 2 parts of catalyst solution were added. After 3 hours, 20 parts of diethynylbenzene and 4 parts of catalyst solution were added. After a total reaction period of 7 hours, gas-liquid chromatographic analysis of the reaction mixture showed that 10% of each of the monomeric components remained. The solution was added to 5 times its volume of methanol, and 77 parts of the copolymer was precipitated. It has an acetylene content of 8.4% and an aromatic to olefin hydrogen ratio of 8:1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04070333 |
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| Source dataset | uspto-grants-1978_01 |
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| ORD ID | ord-3f51c561af8e4f85b216ac55c3c7a370 |
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| Source note | uspto-grants-1978_01 |
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