Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1033583Erstellt: 25. Oktober 2026

N-bromobutanimide → Ethyl 5-bromo-4-(p-chlorophenyl)pyrrole-3-carboxylate

https://huagongshe.com/reaction/1033583

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-bromobutanimideHCID 67184—
Eduktethyl 4-(4-chlorophenyl)-1H-pyrrole-3-carboxylateHCID 470434—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl 5-bromo-4-(p-chlorophenyl)pyrrole-3-carboxylateHCID 1501018590.348,398%

Reaktionsschritte

Ethyl 4-(p-chlorophenyl)pyrrole-3-carboxylate (1.6 g., 0.0064 mmol) is dissolved in tetrahydrofuran (40 mL). N-bromosuccinimide (1.14 g., 0.0064 mmol) is added in small portions at 25°-28° C. After the addition is complete, the solution is stirred overnight at room temperature. The solution is concentrated in vacuo and the solid residue partioned between water and ether. The ether layer is separated and dried over magnesium sulfate. Work-up of the ether extract leaves 1.9 g (90%) of a white solid which is purified by stirring with a mixture of 80/20 hexane/ethyl acetate. The insoluble solid (1.3 g, 62%) is collected and has m.p. 161°-164° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05310938
Quelldatensatzuspto-grants-1994_05
ORD IDord-ad8d558a86874856becc73421c1a1ec8
Quellennotizuspto-grants-1994_05