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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322136Generated: October 28, 2026

4-Methoxybenzaldehyde → HCID 23004054, compound

https://huagongshe.com/reaction/322136

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzaldehydeHCID 31244—
ReactantMethyl 3-aminocrotonateHCID 643918—
ReactantHCID 23004047HCID 23004047—
SolventIsopropanolHCID 3776—
ProductHCID 23004054HCID 23004054—

Reaction Steps

A mixture of 2-cyanoethyl 3-oxohexanoate (11.9 mmol), methyl 3-aminocrotonate (11.9 mmol), and 4-methoxybenzaldehyde in 25 mL of isopropanol is heated at reflux temperature for 16 h, cooled, and the solvent is removed under reduced pressure. The residue is dissolved in 15 mL of dioxane and 626 mg of NaOH in 15 mL of water is added to the reaction mixture. After 0.5 hrs, the solution is concentrated to a small volume under reduced pressure, partitioned between 50 mL of water and 50 mL of ethyl acetate, separated, and the aqueous solution is washed with 2×20 mL of ethyl acetate. The organic solutions are discarded. The aqueous extract is acidified with concentrated HCl (pH=2), and the precipitated oil is extracted with ethyl acetate (2×40 mL). The combined organic extracts are dried (MgSO4), and the solvent is removed in vacuo to give a residue, which is characterized spectroscopically.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211198B1
Source datasetuspto-grants-2001_04
ORD IDord-ba8bfdf759e94c01815fafa0a6336134
Source noteuspto-grants-2001_04