Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066964Generated: October 30, 2026

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

https://huagongshe.com/reaction/1066964

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 numberUS06245773B1
Source datasetuspto-grants-2001_06
ORD IDord-4119453516d0493384c98ee6e4b75079
Source noteuspto-grants-2001_06