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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066963Generated: October 25, 2026

Acetic Acid → Methyl 2-{(3,4-difluorophenyl)methylene}-3-oxobutyrate

https://huagongshe.com/reaction/1066963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethyl acetoacetateHCID 7757—
ReactantPiperidineHCID 8082—
Reactant3,4-DifluorobenzaldehydeHCID 588088—
SolventBenzeneHCID 241—
ProductMethyl 2-{(3,4-difluorophenyl)methylene}-3-oxobutyrateHCID 54038767—

Reaction Steps

A mixture of 3,4-difluorobenzaldehyde (14.2 g, 0.1 mol), methyl acetoacetate (12.2 g, 0.105 mol), piperidine (0.430 g, 5 mmol), and acetic acid (0.30 g, 5 mmol) in benzene (150 mL) was stirred and refluxed with a Dean-Stark trap for 8 hours. Benzene was evaporated, the residue was dissolved in ethyl acetate (200 mL) and washed with brine (50 mL), saturated potassium bisulfate solution (50 mL), and saturated sodium bicarbonate solution in sequence. The ethyl acetate solution was dried (magnesium sulfate), solvent removed under reduced pressure and the residue was purified by column chromatography (SiO2, EtOAc/hexane, 10%-15%). The product, methyl 2-{(3,4-difluorophenyl)methylene}-3-oxobutyrate, was obtained as a yellow oil (0.98 g, 98.3%) and was used in the next step without any further characterization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245773B1
Source datasetuspto-grants-2001_06
ORD IDord-7f2a6b091297446ba014f910005f5a24
Source noteuspto-grants-2001_06