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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1644715Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1644715

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktEthyl AcetateHCID 8857—
Edukt4-Bromo-N,N-dimethylbenzenesulphonamideHCID 12818—
Edukt2-EthynylbenzaldehydeHCID 640368—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelAcetonitrileHCID 6342—
Produkt4-(2-formyl-phenylethynyl)-N,N-dimethyl-benzenesulfonamideHCID 5935085563%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08124629B2
Quelldatensatzuspto-grants-2012_02
ORD IDord-29c8b36c6f7d4c1f91e31f412ae7f1f8
Quellennotizuspto-grants-2012_02