HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18900Erstellt: 23. Oktober 2026
Dichloromethane → N-(2-Benzoyl-4-chloro-phenyl)-4-phenylethynyl-benzenesulfonamide
https://huagongshe.com/de/reaction/18900
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | 1,2-Dimethoxyethane | HCID 8071 | — |
| Edukt | Phenylacetylene | HCID 10821 | — |
| Edukt | N-(2-benzoyl-4-chloro-phenyl)-4-bromo-benzenesulfonamide | HCID 3334757 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Katalysator | Tetrabutylammonium Iodide | HCID 67553 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | N-(2-Benzoyl-4-chloro-phenyl)-4-phenylethynyl-benzenesulfonamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07741519B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-903e7510157140739b126551ce0c9cd1 |
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| Quellennotiz | uspto-grants-2010_06 |
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