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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398930Generated: October 26, 2026

Acetylene → 1,4-Diphenyl-1,3-butadiyne

https://huagongshe.com/reaction/2398930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyleneHCID 6326—
ReactantTriphenylphosphineHCID 11776—
Reactant1,4-Diphenyl-1,3-butadiyneHCID 70174—
Reactant1,2-DiethynylbenzeneHCID 140862—
SolventBenzeneHCID 241—
SolventMethanolHCID 887—
SolventChlorobenzeneHCID 7964—
Product1,4-Diphenyl-1,3-butadiyneHCID 70174—
Product1,4-DiethynylbenzeneHCID 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 nickelacetylacetonate 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 catalystsolution 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 wasprecipitated. It had an acetylene content of 8.4 % and an aromatic to olefin hydrogen ratio of 8:1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04026860
Source datasetuspto-grants-1977_05
ORD IDord-11b61fd5a7744bff91ccedc4d66a0a01
Source noteuspto-grants-1977_05