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HRID 839775作成日:2026年10月25日

Chlorobenzene → Phenylacetylene

https://huagongshe.com/reaction/839775

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorobenzeneHCID 7964—
反応物PhenylacetyleneHCID 10821—
反応物TriphenylphosphineHCID 11776—
触媒Nickel(II) acetylacetonateHCID 9834912—
溶媒BenzeneHCID 241—
生成物PhenylacetyleneHCID 10821—
生成物1,2-DiethynylbenzeneHCID 140862—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04097460
出典データセットuspto-grants-1978_06
ORD IDord-b21e28e6866d411dbc59459847c4c688
出典メモuspto-grants-1978_06