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HRID 24070作成日:2026年10月23日

Tetrahydrofuran → [2-Fluoro-4-(8,8-dimethyl-5-oxo-5,6,7,8-tetrahydronaphthalene-2-ylethynyl)phenyl]acetic acid ethyl ester

https://huagongshe.com/ja/reaction/24070

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Ethyl AcetateHCID 8857—
反応物Ethyl 2-fluoro-4-iodophenylacetateHCID 18740710—
反応物6-ethynyl-3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-oneHCID 22568823—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178418476HCID 178418476—
溶媒HexaneHCID 8058—
生成物[2-Fluoro-4-(8,8-dimethyl-5-oxo-5,6,7,8-tetrahydronaphthalene-2-ylethynyl)phenyl]acetic acid ethyl esterHCID 69548870—

反応手順

Following general procedure F and using 6-ethynyl-4,4-dimethyl-1,2,3,4-tetrahydro-naphthalene-1-one (Intermediate 13, 0.298 g, 1.43 mmol), 2-fluoro-4-iodo phenyl acetic acid ethyl ester (Reagent C, 0.44 g, 1.43 mmol), triethyl amine (Intermediate 13, 3 mL), anhydrous tetrahydrofuran (7mL), copper(I)iodide (0.4 g, 0.2 mmol) and dichlorobis(triphenylphosphine)palladium(II) (0.15 g, 0.213 mmol) followed by flash column chromatography over silica gel (230-400 mesh) using 14-16% ethyl acetate in hexane as the eluent, the title compound was obtained as an oil (0.43 g, 77%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06855512B2
出典データセットuspto-grants-2005_02
ORD IDord-2a4dfa416f764e5f872750375946a95f
出典メモuspto-grants-2005_02