HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978952Generated: October 29, 2026
Methyl p-toluenesulfonate → 2,5-Dimethyl-3,6-diphenyl-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione
https://huagongshe.com/reaction/978952
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl p-toluenesulfonate | HCID 6645 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Dioxo-3,6-diphenylpyrrolo[3,4-c]pyrrole | HCID 15217576 | — |
| Product | 2,5-Dimethyl-3,6-diphenyl-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione | HCID 13803440 | — |
Reaction Steps
14.5 Parts of 1,4-diketo-3,6-diphenylpyrrolo-[3,4-c]-pyrrole, 15 parts of anhydrous potassium carbonate, 40 parts of methyl p-toluenesulfonate and 170 parts of dry nitrobenzene are heated at 200°-205° C. for one hour, with stirring. After cooling to 20° C., the 1,4-diketo-2,5-dimethyl-3,6-diphenylpyrrolo-[3,4-c]-pyrrole obtained is filtered off, washed with toluene, then methanol and thereafter with hot water and dried. 10.85 parts of orange crystals of the compound of the formula (IX) are obtained (melting point 236°-238° C.). ##STR13##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04666455 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-2da64ae9f4614353996865b5ac2fb8f7 |
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| Source note | uspto-grants-1987_05 |
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