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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586127Generated: November 5, 2026

Acetic Acid → Methyl 2-{(benzofuran-5-yl)methylene}-3-oxobutyrate

https://huagongshe.com/reaction/1586127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethyl acetoacetateHCID 7757—
ReactantPiperidineHCID 8082—
ReactantBenzo(c)(1,2,5)oxadiazole-5-carbaldehydeHCID 2776296—
SolventBenzeneHCID 241—
ProductMethyl 2-{(benzofuran-5-yl)methylene}-3-oxobutyrateHCID 54375059—

Reaction Steps

A mixture of 5-Formylbenzofurazan (0.6 g, 4.1 mmol), methyl acetoacetate (0.52 g, 4.5 mmol), piperidine (0.019 g, 0.225 mmol), and acetic acid (0.014 g, 0.225 mmol) in benzene (30 mL) was stirred and refluxed with a Dean-Stark trap for 8 h. Benzene was evaporated, the residue was dissolved in ethyl acetate (80 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{(benzofuran-5-yl)methylene}-3-oxobutyrate, was obtained as an 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 numberUS05942517
Source datasetuspto-grants-1999_08
ORD IDord-25f423bc31da4c73aca2a7e102dd1a98
Source noteuspto-grants-1999_08