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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 6379Erstellt: 23. Oktober 2026

Dimethylformamide → 2-(5-Methoxy-pent-1-yn-1-yl)-benzenesulfonamide

https://huagongshe.com/de/reaction/6379

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
Edukt2-Iodobenzene-1-sulfonamideHCID 2824892—
Edukt5-Methoxypent-1-yneHCID 14221107—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelTriethylamineHCID 8471—
Produkt2-(5-Methoxy-pent-1-yn-1-yl)-benzenesulfonamideHCID 19793626—

Reaktionsschritte

135 ml of N,N-dimethylformamide and 22 ml of triethylamine are taken and 7.5 g of 2-iodobenzenesulfonamide, 2.6 g of pent-4-yn-1-yl-methyl ether as well as 0.067 g of copper(I) iodide and 0.144 g of bis(triphenylphosphine)palladium(II) dichloride are added. The reaction mixture is heated to 65° and stirred for 22 hours at that temperature under argon. After that time, the N,N-dimethylformamide is distilled off at 0.1 torr and 40°. The crude product is purified on 500 g of silica gel (Merck Si 60, 40-63 μm) with hexane/ethyl acetate=2/1 as eluant. The fractions containing the product are concentrated by evaporation at 15 torr and 40° to yield white crystalline 2-(5-methoxy-pent-1-yn-1-yl)-benzenesulfonamide, melting point: 59°-61°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05248693
Quelldatensatzuspto-grants-1993_09
ORD IDord-f88643d947a34b82bf524f131968accd
Quellennotizuspto-grants-1993_09