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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 257553Erstellt: 24. Oktober 2026

Chloride → 2'-(N-t-Butylsulfamoyl)-4-methylbiphenyl

https://huagongshe.com/de/reaction/257553

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorideHCID 312—
EduktStannane, trimethyl(4-methylphenyl)-HCID 617834—
Edukt2-bromo-N-tert-butylbenzenesulfonamideHCID 4825014—
LösungsmittelDimethylformamideHCID 6228—
Produkt2'-(N-t-Butylsulfamoyl)-4-methylbiphenylHCID 1528209974%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

2-Bromo-N-(tert-butyl)benzenesulfonamide (from Step B) (1.00 g, 3.92 mmol), p-tolyltrimethyltin (from Step C) (1.95 g, 6.67 mmol), bis(triphenylphosphinepalladium(II) chloride (Aldrich) (165 mg, 0.235 mmol) and dimethylformamide (25 ml) were heated with stirring under nitrogen at 90° C. for 5 hours. The black suspension was cooled to room temperature, then filtered through a pad of Celite which was washed with tetrahydrofuran. The colorless filtrate was evaporated to dryness, then chromatographed (silica gel, 10% ethyl acetate-hexane) to give the title compound (0.88 g, 74%) as a white solid; 1H NMR (300 MHz, CDCl3) δ8.16 (d, J=7.9 Hz, 1H), 7.60-7.37 (m, 4H), 7.36-7.24 (m, 3H), 3.57 (s, 1H), 2.42 (s, 3H), 0.99 (s, 9H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05262412
Quelldatensatzuspto-grants-1993_11
ORD IDord-96b8bbb5fb2546eea284fbd01e5920c3
Quellennotizuspto-grants-1993_11