HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259441Generated: October 29, 2026
Hydrochloric Acid → 2-(4-Carboxyphenyl)-1-dimethylamino-4-phenyl-1-butene-3,4-dione
https://huagongshe.com/reaction/259441
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | HCID 20304493 | HCID 20304493 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(4-Carboxyphenyl)-1-dimethylamino-4-phenyl-1-butene-3,4-dione | HCID 54061069 | 44% |
Reaction Steps
To a solution of 3-(4-carboxyphenyl)-1-phenyl-1,2-propanedione in 100 ml of dry dimethylformamide cooled in an ice-bath was added, with stirring, 56 ml of dimethylformamide dimethyl acetal. The reaction mixture was stirred at 0°-5° C. for 10 min. and then it was poured onto 1.2 l. of ice-water and acidified with 130 ml of 1N hydrochloric acid. After stirring for 5 min., 1.8 l. of water was added and the precipitate was collected, washed with water and air-dried. The filter cake was dissolved in 1.7 l. of methylene chloride, dried over anhydrous sodium sulfate, filtered and the filtrate was concentrated to about 200 ml. Ether (200 ml) was added and the solution was concentrated to about 300 ml and allowed to stand at room temperature for 2 days. The solid was collected, washed with methylene chloride-ether (1:9) and dried at 80° C. for 3 hrs. to give 17.4 g (44%) of 2-(4-carboxyphenyl)-1-dimethylamino-4-phenyl-1-butene-3,4-dione as yellow crystals, m.p. 208°-209° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04038289 |
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| Source dataset | uspto-grants-1977_07 |
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| ORD ID | ord-32bd1fc2bb0f4cd181dec7da60a7e83b |
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| Source note | uspto-grants-1977_07 |
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