HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978959Generated: October 31, 2026
Dimethylformamide → HCID 20201047, compound
https://huagongshe.com/reaction/978959
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethyl p-methylbenzenesulfonate | HCID 6638 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Dioxo-3,6-diphenylpyrrolo[3,4-c]pyrrole | HCID 15217576 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 20201047 | HCID 20201047 | — |
Reaction Steps
A solution of 16 parts of ethyl toluene-4-sulfonate in 15 parts of dimethylformamide is added to a mixture, warmed to 140°-142° C., of 5.8 parts of 1,4-diketo-3,6-diphenylpyrrolo-[3,4-c]-pyrrole, 12.2 parts of potassium carbonate and 60 parts of dimethylformamide in the course of 30 minutes, with stirring. The brown-yellow solution formed is subsequently stirred at 142° C. for 5 minutes, and 100 parts of methanol are added at 70° C. The yellow precipitate which has separated out is filtered off at 15° C., washed with methanol and with hot water at 90° C. and dried. The crude product (3.6 parts) is recrystallised first from 40 part of dimethylformamide and then from 100 parts of n-butanol. 2.8 parts of 1,4-diketo-2,5-diethyl-3,6-diphenylpyrrolo-[3,4-c]-pyrrole of the following formula are obtained in the form of orange-yellow needles of melting point 229°-230° C.: ##STR32##
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-57a73f72232049e0ae771b14aa753baf |
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| Source note | uspto-grants-1987_05 |
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