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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643584Generated: October 30, 2026

Hydrochloric Acid → 3-(3,4-dichlorophenyl)-2-oxopropanoic acid

https://huagongshe.com/reaction/643584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantTolueneHCID 1140—
Reactant2-acetylamino-3-(3,4-dichloro-phenyl)-acrylic acidHCID 2747201—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product3-(3,4-dichlorophenyl)-2-oxopropanoic acidHCID 15024029—

Reaction Conditions

Temperature125 °C

Reaction Steps

140 mL 4 M HCl were added to a suspension of 21.0 g (76.6 mmol) 2-acetylamino-3-(3,4-dichloro-phenyl)-acrylic acid in 100 mL N-methyl-2-pyrrolidinone and the reaction mixture was then heated for 4 h at an oil bath temperature of 125° C. The cooled reaction solution was poured onto a cooled mixture of 350 mL water and 120 mL toluene. The phases were separated, the aqueous phase was again extracted with toluene, the combined organic phases were extracted with water, filtered through Na2SO4 and evaporated down i. vac. The residue was taken up in 1 M NaOH and washed twice with diethyl ether. The aqueous phase was acidified with 2 M HCl and extracted three times with EtOAc. The combined organic phases were filtered through Na2SO4 and evaporated down i. vac. The residue was combined with diethyl ether, suction filtered and dried in the vacuum drying cupboard.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700598B2
Source datasetuspto-grants-2010_04
ORD IDord-42cf452218e943dbab968ef9fcf8e669
Source noteuspto-grants-2010_04