Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387849Generated: October 29, 2026

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

https://huagongshe.com/reaction/2387849

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 numberUS08268990B2
Source datasetuspto-grants-2012_09
ORD IDord-065d6b5f09fe4b41bcc5fd86bcbd7d5a
Source noteuspto-grants-2012_09