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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869049Generated: October 29, 2026

Acetic Acid → 1-(3-Chloro-2-fluoro-phenyl)-5-(4-chloro-phenyl)-3-hydroxy-4-isobutyryl-1,5-dihydro-pyrrol-2-one

https://huagongshe.com/reaction/869049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-ChlorobenzaldehydeHCID 7726—
Reactant3-Chloro-2-fluoroanilineHCID 75014—
ReactantEthyl 5-methyl-2,4-dioxohexanoateHCID 3017501—
ReactantSodiumHCID 5360545—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product1-(3-Chloro-2-fluoro-phenyl)-5-(4-chloro-phenyl)-3-hydroxy-4-isobutyryl-1,5-dihydro-pyrrol-2-oneHCID 8960243148.3%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 3-chloro-2-fluoro-aniline (10.9 g, 75 mmol) and 4-chloro-benzaldehyde (10.0 g, 71 mmol) was heated to 120° C., stirred for 18 h, allowed to cool to rt, and diluted with toluene (50 mL). A mixture of the sodium salt of 5-methyl-2,4-dioxo-hexanoic acid ethyl ester (14.8 g, 71 mmol) in dioxane (50 mL) and acetic acid (4.1 mL, 71 mmol) was added. The resulting mixture was refluxed for 18 h, allowed to cool to rt, diluted with EtOAc, and washed twice with an aqueous solution of NaHCO3 and brine. The crude product, obtained after drying and concentration, was triturated with EtOAc/hexane to provide 14 g of the title compound. tR: 5.23 min (HPLC 1); ESI-MS: 408 [M+H]+ (LC-MS1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969341B2
Source datasetuspto-grants-2015_03
ORD IDord-7efad27c4cae4c95b1355cb632814a3e
Source noteuspto-grants-2015_03