戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1011866作成日:2026年10月26日

1-Hexyne → 3,5-Diethyl-1-(3-hex-1-ynyl-phenyl)-1H-pyrazole-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/1011866

反応式

関与物質

役割名称HCID仕込み量
反応物1-HexyneHCID 12732—
反応物1-(3-Bromo-phenyl)-3,5-diethyl-1H-pyrazole-4-carboxylic acid methyl esterHCID 67313992—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒PiperidineHCID 8082—
生成物3,5-Diethyl-1-(3-hex-1-ynyl-phenyl)-1H-pyrazole-4-carboxylic acid methyl esterHCID 67314187—

反応条件

温度60 °C

反応手順

A solution of 4.20 g (10.0 mmol) of 1-(3-bromo-phenyl)-3,5-diethyl-1H-pyrazole-4-carboxylic acid methyl ester (intermediate 1C) in 35 ml of piperidine was treated with 0.19 g (1.0 mmol) of copper(I)iodide and 1.16 g (1.0 mmol) of tetrakis-(triphenylphosphine)-palladium. The reaction mixture was warmed up to 60° C. and after 15 min, a solution of 0.82 g=1.00 ml (10.0 mmol) of hex-1-yne in 15 ml of piperidine was added drop by drop during 1 hour. After 30 min, the oil bath temperature was steadily increased to 80° C. The reaction mixture was then stirred at 80° C. for 4 hours, and subsequently cooled down to RT. The solvent was evaporated and the residue poured into crashed ice, acidified with HCl (37%) to pH 1-2 and extracted twice with EtOAc; the organic phases were washed with water, dried over magnesium sulfate, filtered and evaporated. The residue was purified by flash column chromatography (n-heptane:EtOAc 1:0-9:1) to afford the title compound as light yellow oil. MS: 339.0 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07977358B2
出典データセットuspto-grants-2011_07
ORD IDord-136b20bce9594ee99e6b6b12daba7ba8
出典メモuspto-grants-2011_07