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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732689Generated: October 31, 2026

Hydrochloric Acid → 2-(4-Carboxyphenyl)-1-dimethylamino-4-phenyl-1-butene-3,4-dione

https://huagongshe.com/reaction/1732689

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 1 N 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 numberUS04238589
Source datasetuspto-grants-1980_12
ORD IDord-f617c73aeffd4550b74e99cf11f8ef5f
Source noteuspto-grants-1980_12