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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2-Thiophenecarbonitrile | HCID 66087 | — |
| Reactant | Diisopropyl succinate | HCID 70213 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Catalyst | Iron chloride (FeCl3) | HCID 24380 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 2-Methyl-2-butanol | HCID 6405 | — |
| Product | 1,4-dithiophen-2-yl-2,5-dihydropyrrolo[3,4-c]pyrrole-3,6-dione | HCID 178517529 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08624232B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-9346b47952254f16ac1197b02b0ba919 |
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| Source note | uspto-grants-2014_01 |
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