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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1644715생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1644715

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl AcetateHCID 8857—
반응물4-Bromo-N,N-dimethylbenzenesulphonamideHCID 12818—
반응물2-EthynylbenzaldehydeHCID 640368—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매AcetonitrileHCID 6342—
생성물4-(2-formyl-phenylethynyl)-N,N-dimethyl-benzenesulfonamideHCID 5935085563%

반응 조건

온도80 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08124629B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-29c8b36c6f7d4c1f91e31f412ae7f1f8
출처 메모uspto-grants-2012_02