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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 749232Erstellt: 25. Oktober 2026

Triethylamine → 3-[4-[(6-Bromohexyl)oxy]but-1-ynyl}benzenesulfonamide

https://huagongshe.com/reaction/749232

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt3-Bromobenzene-1-sulfonamideHCID 2734765—
Edukt6-Bromohexylbut-3-ynyl etherHCID 11379281—
KatalysatorTriphenylphosphineHCID 11776—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorDichlorobis(triphenylphosphine)palladiumHCID 6102075—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-[4-[(6-Bromohexyl)oxy]but-1-ynyl}benzenesulfonamideHCID 2189555890,7%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A mixture of 3-bromo-benzenesulfonamide (625 g), 6-bromohexyl but-3-ynyl ether (850.1 g), bis(triphenylphosphine)palladium (II) chloride (62.5 g), triphenylphosphine (18.1 g) and triethylamine (536.3 g) in tetrahydrofuran (6250 ml) was stirred under an atmosphere of nitrogen for 20 min. Copper (I) iodide (12.5 g) was then added to give a dark red/brown mixture that was heated to 50° C. for 23 h. The reaction mixture was then cooled to room temperature and filtered through a short silica pad (1000 g). The pad was washed with additional tetrahydrofuran (15.6L) and the resulting solution then concentrated under reduced pressure to give crude product (1382 g) as a viscous oil. This was purified by chromatography (7 kg silica) eluting with petroleum ether-ethyl acetate (5:1) followed by petroleum ether-ethyl acetate (2:1) to give the title compound (932.9 g) as an oil, LC RT=5.69 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07402598B2
Quelldatensatzuspto-grants-2008_07
ORD IDord-5a7b2cd47f7f43738379bbc82be57700
Quellennotizuspto-grants-2008_07