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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 327832Erstellt: 24. Oktober 2026

Pyrrole-2-Carboxylic Acid → 2-[2-(1H-Pyrrol-2-ylcarbonyl)-1H-pyrrol-1-yl]-1H-isoindole-1,3(2H)dione

https://huagongshe.com/de/reaction/327832

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyrrole-2-Carboxylic AcidHCID 12473—
EduktTin tetrachlorideHCID 24287—
EduktOxalyl chlorideHCID 65578—
Edukt2-(1H-Pyrrol-1-yl)isoindoline-1,3-dioneHCID 853719—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-[2-(1H-Pyrrol-2-ylcarbonyl)-1H-pyrrol-1-yl]-1H-isoindole-1,3(2H)dioneHCID 1997317869,2%

Reaktionsbedingungen

Temperatur-10 °C

Reaktionsschritte

To a suspension of pyrrole-2-carboxylic acid (5.55 g) in 500 ml of DCM was added oxalyl chloride (8.7). The reaction mixture was heated under reflux for 1 hour, cooled to -10° C., and tin (IV) chloride (5.85 ml) was added. After stirring the mixture at -10° C. for 30 minutes, 2-(1H-pyrrol-1-yl)-1H-isoindole-1,3(2H)dione (10.6 g) was added in four portions over a period of 30 minutes, followed by stirring at -10° C. for additional 30 minutes. The reaction mixture was then poured into 500 ml of water and extracted with DCM. The combined extracts were washed with 1N sodium hydroxide solution, 1N sulfuric acid, and finally with water. The dried (magnesium sulfate) organic phase was filtered and evaporated in vacuo. The residue was triturated with DCM, affording the product as a powder (10.55 g), mp 204°-206° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05274116
Quelldatensatzuspto-grants-1993_12
ORD IDord-2d0ba08bcd8948fe910437103829fd42
Quellennotizuspto-grants-1993_12