戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 51731作成日:2026年10月27日

4-Ethynyl-1-(1-isopropoxycyclopropyl)-3-methyl-benzene → Ethyl4-[4-(1-isopropoxycyclopropyl)-3-methyl-phenylethynyl]-benzoate

https://huagongshe.com/reaction/51731

反応式

関与物質

役割名称HCID仕込み量
反応物4-Ethynyl-1-(1-isopropoxycyclopropyl)-3-methyl-benzeneHCID 22568997—
反応物Ethyl-4-iodo-benzoate benzoateHCID 69887287—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178418476HCID 178418476—
溶媒TriethylamineHCID 8471—
生成物Ethyl4-[4-(1-isopropoxycyclopropyl)-3-methyl-phenylethynyl]-benzoateHCID 22568844159.2%

反応手順

Using General Procedure F; 4-ethynyl-1-(1-isopropoxycyclopropyl)-3-methyl-benzene (Intermediate 81, 80.0 mg, 0.13 mmol) and ethyl-4-iodo benzoate (Reagent A, 100.0 mg, 0.36 mmol) in triethylamine (5 mL) was treated with copper(I)iodide (25.0 mg, 0.13 mmol) and sparged with argon for 5 minutes. Dichlorobis(triphenylphosphine)-palladium(II) (91 mg, 0.13 mmol) was added and the reaction mixture was stirred overnight at room temperature. Column chromatography (2-4% EtOAc-hexanes) afforded 75.0 mg (56%) of the title compound as an orange solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713647B2
出典データセットuspto-grants-2004_03
ORD IDord-8fadf66058e54861ba260ff04d8d7272
出典メモuspto-grants-2004_03