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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371419Generated: November 1, 2026

Acetic Acid → HCID 54106535, compound

https://huagongshe.com/reaction/371419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethyl acetoacetateHCID 7757—
ReactantPiperidineHCID 8082—
Reactant2-[(4-Methylbenzyl)oxy]benzaldehydeHCID 693304—
SolventIsopropanolHCID 3776—
ProductHCID 54106535HCID 54106535—

Reaction Conditions

Temperature40 °C

Reaction Steps

25 g (110.6 millimols) of 2-(4-methylbenzyloxy)-benzaldehyde were stirred with 11.9 ml (110.6 millimols) of methyl acetoacetate in 66 ml of isopropanol, and a freshly prepared solution of 0.64 ml of piperidine and 0.38 ml of glacial acetic acid in 5.5 ml of isopropanol was added. The mixture was stirred for 1 hour at 60° C. and for 4 hours at 40° C., and was cooled and concentrated. The residue from evaporation was dissolved in ether, and the solution was washed successively with approx. 100 ml of 1N hydrochloric acid, with two portions of water, with saturated sodium bicarbonate solution and again with two portions of water. The ether phase was dried, filtered and concentrated. 35.3 g (98.51% of theory) of a dark yellow oil were obtained, and the oil was reacted further in the crude form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04532248
Source datasetuspto-grants-1985_07
ORD IDord-b9062448f74042daae58b47f4470955f
Source noteuspto-grants-1985_07