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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1765527Erstellt: 26. Oktober 2026

Dichloromethane → N-(2-Benzoyl-4-chloro-phenyl)-4-phenylethynyl-benzenesulfonamide

https://huagongshe.com/reaction/1765527

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
Edukt1,2-DimethoxyethaneHCID 8071—
EduktPhenylacetyleneHCID 10821—
EduktN-(2-benzoyl-4-chloro-phenyl)-4-bromo-benzenesulfonamideHCID 3334757—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorTetrabutylammonium IodideHCID 67553—
LösungsmittelTriethylamineHCID 8471—
ProduktN-(2-Benzoyl-4-chloro-phenyl)-4-phenylethynyl-benzenesulfonamideHCID 11328918—

Reaktionsschritte

To a magnetically stirred mixture of the N-(2-Benzoyl-4-chloro-phenyl)-4-bromo-benzenesulfonamide (450 mg, 1.0 mmol), [1,1′ Bis-(diphenylphosphino)ferrocene]dichloropalladium(II) complex with dichloromethane (1:1) (30 mg, 0.037 mmol) and copper (I) iodide (100 mg, 0.52 mmol) was added DME (6 mL) and dry triethylamine (3 mL) under dry nitrogen. To this stirred mixture was added tetrabutylammonium iodide (250 mg), followed by the addition of phenylacetylene (0.240 mL). The dark green mixture was stirred at ambient temp overnight. The reaction was worked up by addition to crushed ice and extracted with ethyl acetate (3×75 mL), and the organic layer was dried (MgSO4), filtered and concentrated. The crude product was chromatographed on silica gel using 10–30% EtOAc/Hexane. 1H NMR (CDCl3) δ 9.64 (br s, 1H, NH), 7.75 (d, 1H, J=Hz), 7.75 (d, 1H, J=8.8 Hz), 7.48 (m, 8H), 7.36 (m, 7H). MS: m/z 472 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07227035B2
Quelldatensatzuspto-grants-2007_06
ORD IDord-a558f353168040449fb18fc3c4c1d9ea
Quellennotizuspto-grants-2007_06