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HRID 1470640作成日:2026年10月26日

4-Ethynyl-1,1'-biphenyl → 2-Amino-3-biphenyl-4-ylethynyl-benzoic acid methyl ester

https://huagongshe.com/reaction/1470640

反応式

関与物質

役割名称HCID仕込み量
反応物4-Ethynyl-1,1'-biphenylHCID 34464—
反応物Methyl 2-amino-3-iodobenzoateHCID 21258150—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
溶媒TetrahydrofuranHCID 8028—
生成物2-Amino-3-biphenyl-4-ylethynyl-benzoic acid methyl esterHCID 6670634276.4%

反応手順

To a solution of 2-amino-3-iodo-benzoic acid methyl ester (500 mg, 1.8 mmol), 4-ethynyl-biphenyl (416 mg, 2.3 mmol) in THF (20 mL), CuI (17 mg, 0.09 mmol), bis-(triphenylphosphine)-palladium (II)-chloride (64 mg, 0.09 mmol) and TEA (0.75 mL, 5.4 mmol) were added. This mixture was stirred at room temperature for 12 h. The progress of the reaction was monitored by TLC. After completion, the reaction mass was filtered through celite, and the collected filtrate was diluted with ethyl acetate (30 mL), washed with water (2×20 mL) and the combined organic layer was separated and dried over sodium sulphate and concentrated under reduced pressure to obtain brown mass which was purified by column chromatography using 5% ethyl acetate in hexane as an eluent to obtain 450 mg of 2-amino-3-biphenyl-4-ylethynyl-benzoic acid methyl ester as a pale yellow coloured solid (76%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09006454B2
出典データセットuspto-grants-2015_04
ORD IDord-ec4b4a98675e4a7e8de6f7f7588ea4e5
出典メモuspto-grants-2015_04