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HRID 1644715作成日:2026年10月27日

Triethylamine → 4-(2-formyl-phenylethynyl)-N,N-dimethyl-benzenesulfonamide

https://huagongshe.com/reaction/1644715

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ethyl AcetateHCID 8857—
反応物4-Bromo-N,N-dimethylbenzenesulphonamideHCID 12818—
反応物2-EthynylbenzaldehydeHCID 640368—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒AcetonitrileHCID 6342—
生成物4-(2-formyl-phenylethynyl)-N,N-dimethyl-benzenesulfonamideHCID 5935085563%

反応条件

温度80 °C

反応手順

A mixture of 4-bromo-N,N-dimethylbenzenesulfonamide (610 mg, 2.31 mmol) bis(triphenylphosphine)palladium(II) chloride (Pd(PPh3)2Cl2) (33 mg, 0.05 mmol), copper (I) iodide (5 mg, 0.03 mmol) and triethylamine (3 mL) was degassed with argon. To the above mixture was added a degassed solution of 2-ethynyl-benzaldehyde (300 mg, 2.31 mmol) in acetonitrile (3 mL). The resulting mixture was heated at 80° C. for 3 hours under argon, and then cooled to room temperature, treated with ethyl acetate, and then washed with water. The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (RediSep® Flash column, 230-400 mesh, 5-40% ethyl acetate in hexane) gave 4-(2-formyl-phenylethynyl)-N,N-dimethyl-benzenesulfonamide (454 mg, 63%) as a brown oil. MS (ESI+) cald. for C17H15NO3S [(M+H)+] 313, obsd. 314.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08124629B2
出典データセットuspto-grants-2012_02
ORD IDord-29c8b36c6f7d4c1f91e31f412ae7f1f8
出典メモuspto-grants-2012_02