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HRID 51740作成日:2026年10月26日

1-Ethynyl-4-(1-benzyloxycyclopropyl)-3-ethyl-benzene → Ethyl4-[4-(1-benzyloxycyclopropyl)-3-ethyl-phenylethynyl]-benzoate

https://huagongshe.com/reaction/51740

反応式

関与物質

役割名称HCID仕込み量
反応物1-Ethynyl-4-(1-benzyloxycyclopropyl)-3-ethyl-benzeneHCID 22568983—
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-benzyloxycyclopropyl)-3-ethyl-phenylethynyl]-benzoateHCID 2256899272%

反応手順

Using General Procedure F; 1-ethynyl-4-(1-benzyloxycyclopropyl)-3-ethyl-benzene (Intermediate 90, 90.0 mg, 0.33 mmol) and ethyl-4-iodo benzoate (Reagent A, 100.0 mg, 0.36 mmol) in triethylamine (5 mL) was treated with copper(I)iodide (21.0 mg, 0.11 mmol) and sparged with argon for 5 minutes. Dichlorobis(triphenylphosphine)palladium(II) (77 mg, 0.11 mmol) was added and the reaction mixture was stirred overnight at room temperature. Column chromatography (2-4% EtOAc-hexanes) afforded 100.0 mg (72%) of the title compound.

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-1b781f55accc43c9b1b27ad6a6104566
出典メモuspto-grants-2004_03