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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantDimethylformamide dimethyl acetalHCID 78373—
ReactantHCID 20304493HCID 20304493—
SolventDimethylformamideHCID 6228—
Product2-(4-Carboxyphenyl)-1-dimethylamino-4-phenyl-1-butene-3,4-dioneHCID 5406106944%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04038289
Source datasetuspto-grants-1977_07
ORD IDord-32bd1fc2bb0f4cd181dec7da60a7e83b
Source noteuspto-grants-1977_07