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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1617197Generated: November 2, 2026

Acetic Acid → Ethyl 2-(4-(benzyloxy)-2-methoxybenzylidene)-3-oxobutanoate

https://huagongshe.com/reaction/1617197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPiperidineHCID 8082—
ReactantEthyl AcetoacetateHCID 8868—
Reactant4-Benzyloxy-2-methoxybenzaldehydeHCID 4293990—
SolventTolueneHCID 1140—
ProductEthyl 2-(4-(benzyloxy)-2-methoxybenzylidene)-3-oxobutanoateHCID 68413560—

Reaction Steps

A solution of 4-(benzyloxy)-2-methoxybenzaldehyde (28.3 g), ethyl acetoacetate (18 ml), acetic acid (1.74 ml) and piperidine (0.56 ml) in toluene (400 ml) was heated under reflux for 48 h. A solution of acetic acid (1.74 ml) and piperidine (0.56 ml) in toluene (10 ml) was added and the solution heated under reflux for a further 48 h. The solvent was evaporated under reduced pressure and the residue partitioned between EtOAc and brine. The organics were separated, washed with aq NaHCO3 soln, 1M HCl, brine, dried and evaporated under reduced pressure to give the subtitle compound, 40 g (used crude in next step).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765939B2
Source datasetuspto-grants-2014_07
ORD IDord-8c3b35087a9d44139bbd1eeef3e43e1c
Source noteuspto-grants-2014_07