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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 468707Erstellt: 24. Oktober 2026

Acetic Acid → 1,4-dithiophen-2-yl-2,5-dihydropyrrolo[3,4-c]pyrrole-3,6-dione

https://huagongshe.com/de/reaction/468707

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt2-ThiophenecarbonitrileHCID 66087—
EduktDiisopropyl succinateHCID 70213—
EduktSodiumHCID 5360545—
KatalysatorIron chloride (FeCl3)HCID 24380—
LösungsmittelMethanolHCID 887—
Lösungsmittel2-Methyl-2-butanolHCID 6405—
Produkt1,4-dithiophen-2-yl-2,5-dihydropyrrolo[3,4-c]pyrrole-3,6-dioneHCID 178517529—

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

Sodium metal (6.90 g, 0.30 mol) was added to 100 ml t-amyl alcohol and a small amount of iron (III) chloride (100 mg) was added. The mixture was stirred vigorously for 2 hr at 105° C. until the sodium dissolved. The solution was cooled to 85° C. and 2-thiophenecarbonitrile (22.0 g, 0.2 mol) was added. Diisopropyl succinate (16.6 g, 0.08 mol) dissolved in 10 ml of t-amyl alcohol was added dropwise to the reaction mixture over 1 hr at 85° C. The reaction mixture was stirred at this temperature for 12 hrs, then cooled to 50° C., diluted with 100 ml of methanol, and then slowly neutralized with 30 ml of glacial acetic acid and refluxed briefly, and then filtered. The residue was washed several times with hot methanol and water, and the resultant solid was dried in a vacuum oven at 50° C. A dark red color powder was obtained which was used without further purification (20 g, 83%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08624232B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-9346b47952254f16ac1197b02b0ba919
Quellennotizuspto-grants-2014_01