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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 413894Erstellt: 24. Oktober 2026

p-Toluenesulfonic acid → 1-(3-Methanesulfonylphenyl)-2-methyl-5-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester

https://huagongshe.com/de/reaction/413894

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Toluenesulfonic acidHCID 6101—
EduktTriethylamineHCID 8471—
EduktEthyl 2-acetyl-4-oxo-4-phenylbutanoateHCID 312893—
Edukt3-(Methylsulphonyl)anilineHCID 428029—
LösungsmittelEthanolHCID 702—
LösungsmittelChloroformHCID 6212—
Produkt1-(3-Methanesulfonylphenyl)-2-methyl-5-phenyl-1H-pyrrole-3-carboxylic acid ethyl esterHCID 10134575—

Reaktionsschritte

3-Methylsulfonylaniline (1.4 mmol, 0.3 g), 3-oxo-2-(2-oxo-2-phenyl-ethyl)-butyric acid ethyl ester (1.4 mmol, 0.35 g), triethylamine (1.4 mmol, 0.14 g), and tosic acid (0.1 g) were combined in ethanol, then heated under reflux. The resulting oil was resuspended in chloroform, then washed with water, 5% sodium bicarbonate, and brine. The organic layer was dried over NaSO4, then the solids were separated and the solvents removed under vacuum. The crude material was purified over silica gel to yield the named product as an oil. The structure of the compound was verified by 1H-NMR (CDCl3, ppm): 1.36 t (3H), 2.45 s (3H), 2.82 s (3H), 4.3 q (2H), and 6.8-7.2 m (9H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06569890B2
Quelldatensatzuspto-grants-2003_05
ORD IDord-112f49d5fca64863ae250c0626d3f28f
Quellennotizuspto-grants-2003_05