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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 565211Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/565211

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktMethyl acetoacetateHCID 7757—
EduktPiperidineHCID 8082—
Edukt3,4-DifluorobenzaldehydeHCID 588088—
LösungsmittelBenzeneHCID 241—
ProduktMethyl 2-{(3,4-difluorophenyl)methylene}-3-oxobutyrateHCID 54038767—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06172066B2
Quelldatensatzuspto-grants-2001_01
ORD IDord-5df532d729104adbbf6d14463badf70f
Quellennotizuspto-grants-2001_01