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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468707Generated: October 26, 2026

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

https://huagongshe.com/reaction/468707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-ThiophenecarbonitrileHCID 66087—
ReactantDiisopropyl succinateHCID 70213—
ReactantSodiumHCID 5360545—
CatalystIron chloride (FeCl3)HCID 24380—
SolventMethanolHCID 887—
Solvent2-Methyl-2-butanolHCID 6405—
Product1,4-dithiophen-2-yl-2,5-dihydropyrrolo[3,4-c]pyrrole-3,6-dioneHCID 178517529—

Reaction Conditions

Temperature85 °C

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08624232B2
Source datasetuspto-grants-2014_01
ORD IDord-9346b47952254f16ac1197b02b0ba919
Source noteuspto-grants-2014_01