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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 842183Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/842183

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
PatentnummerUS06372777B1
Quelldatensatzuspto-grants-2002_04
ORD IDord-6080381e422f4d8da4bde78b3864aff0
Quellennotizuspto-grants-2002_04