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HRID 395052作成日:2026年10月24日

Tetrahydrofuran → [2-Fluoro-4-(2,2,4,4-tetramethyl-chroman-6-ylethynyl) phenyl]acetic acid ethyl ester

https://huagongshe.com/ja/reaction/395052

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物TriethylamineHCID 8471—
反応物2,2,4,4-Tetramethyl-6-ethynylchromanHCID 15661138—
反応物Ethyl 2-fluoro-4-iodophenylacetateHCID 18740710—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178418476HCID 178418476—
溶媒HexaneHCID 8058—
溶媒Ethyl AcetateHCID 8857—
生成物[2-Fluoro-4-(2,2,4,4-tetramethyl-chroman-6-ylethynyl) phenyl]acetic acid ethyl esterHCID 69548829—

反応手順

Following general procedure F and using 6-ethynyl-2,2,4,4-tetramethylchroman (0.204 g, 0.95 mmol), ethyl-2-fluoro-4-iodo phenyl acetate (Reagent C, 0.263 g, 0.86 mmol), triethyl amine, tetrahydrofuran, copper(I)iodide (0.025 g, 0.13 mmol) and dichlorobis(triphenylphosphine)palladium(II) (0.075 g, 0.11 mmol) followed by flash column chromatography over silica gel (230-400 mesh) using 5-10% ethyl acetate in hexane as the eluent, the title compound was obtained (0.21 g, 62%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06603019B2
出典データセットuspto-grants-2003_08
ORD IDord-812228214d814c70924c10ba3bf81f12
出典メモuspto-grants-2003_08