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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549481Generated: October 28, 2026

Hydrochloric Acid → HCID 57440925, compound

https://huagongshe.com/reaction/549481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetic AnhydrideHCID 7918—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzeneacetic acid, 4-bromo-HCID 74654—
Reactant4-Chloro-2-nitrobenzaldehydeHCID 79674—
SolventWaterHCID 962—
ProductHCID 57440925HCID 5744092558.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

A 2 L flask equipped with a mechanical stirrer was charged with 183 g of 2-nitro-4-chlorobenzaldehyde, 212 g of 4-bromophenylacetic acid and 233 mL of acetic anhydride. To this solution was added 82 g of potassium carbonate and the reaction was stirred overnight at 100° C. The resulting dark mixture was cooled down to room temperature and 1.6 L of water was added followed by 800 mL of 10% HCl. The solution was decanted and taken up in water/ethyl acetate. Layers were separated, organic phase was washed with brine, dried over magnesium sulphate and volatiles were removed under reduced pressure. The residue was triturated in EtOH and the mother liquor was triturated 4 more times with EtOH to afford 219 g of the desired (2E)-2-(4-bromophenyl)-3-(4-chloro-2-nitrophenyl)acrylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943649B2
Source datasetuspto-grants-2011_05
ORD IDord-eea4f2219de747519cbcd53cddf64dd8
Source noteuspto-grants-2011_05