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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840321Generated: October 28, 2026

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

https://huagongshe.com/reaction/1840321

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 numberUS06680323B2
Source datasetuspto-grants-2004_01
ORD IDord-80a5d937c0024fe68d384d1a0d579691
Source noteuspto-grants-2004_01