戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 71210作成日:2026年10月24日

Triethylamine → 5-[4-(5-Chloropent-1-yn-1-yl)-2-methoxyphenyl]-2-methyl-1,3-oxazole

https://huagongshe.com/ja/reaction/71210

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1-Pentyne, 5-chloro-HCID 84308—
反応物5-(4-Bromo-2-methoxyphenyl)-2-methyloxazoleHCID 66608732—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178418476HCID 178418476—
溶媒Ethyl AcetateHCID 8857—
生成物5-[4-(5-Chloropent-1-yn-1-yl)-2-methoxyphenyl]-2-methyl-1,3-oxazoleHCID 66608267—

反応条件

温度70 °C

反応手順

A mixture of 5-(4-bromo-2-methoxyphenyl)-2-methyl-1,3-oxazole (6.00 g), 5-chloropent-1-yne (4.74 mL), dichlorobis(triphenylphosphine)palladium(II) (1.57 g), copper(I) iodide (426 mg) and triethylamine (60 mL) was stirred at 70° C. for 3 hr, and diluted with ethyl acetate, and the mixture was filtered through celite. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (4.85 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822699B2
出典データセットuspto-grants-2014_09
ORD IDord-4cc6270886fc4692977c650aa62d336b
出典メモuspto-grants-2014_09