戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 128809作成日:2026年10月24日

Phenylacetylene → 4-(Phenylethynyl)benzaldehyde

https://huagongshe.com/ja/reaction/128809

反応式

関与物質

役割名称HCID仕込み量
反応物PhenylacetyleneHCID 10821—
反応物4-BromobenzaldehydeHCID 70741—
触媒Palladium(2+) acetate--triphenylphosphane (1/2/2)HCID 84538—
生成物4-(Phenylethynyl)benzaldehydeHCID 60990870%

反応手順

By the method of example 53(A), but using bis(triphenylphosphine)palladium(II) acetate as catalyst (3 mol %), phenylacetylene and 4-bromobenzaldehyde are coupled to give 4-(2-phenylethynyl)benzaldehyde in 70% yield after distillation. By the methods of example 1, this is converted into the title compound, obtained as a colorless solid, mp 190°-191° after recrystallization from hexane-ethyl acetate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05464865
出典データセットuspto-grants-1995_11
ORD IDord-843acba50177435e8a47409e0d2ace33
出典メモuspto-grants-1995_11