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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086819Generated: November 1, 2026

Acetic Acid → HCID 54092388, compound

https://huagongshe.com/reaction/1086819

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPiperidineHCID 8082—
Reactant3-Methyl-2-butanoneHCID 11251—
Reactant4-Fluoro-3-phenoxybenzaldehydeHCID 110068—
ReactantEthyl 5-methyl-4-oxohexanoateHCID 12892835—
SolventIsopropanolHCID 3776—
ProductHCID 54092388HCID 54092388—

Reaction Steps

2.8 ml (29 mmol) of piperidine and 1.7 ml (29 mmol) of acetic acid are added to a solution of 79 g (0.5 mol) of ethyl 4-methyl-3-oxo-pentanecarboxylate (prepared from methyl isopropyl ketone analogously to the process of S. B. Soloway and F. B. La Forge, J. Am. Chem. Soc. 69, 2677 (1947)) and 108 g (0.5 mol) of 4-fluoro-3-phenoxy-benzaldehyde in 300 ml of isopropanol and stirred overnight at RT. The mixture is then concentrated, the residue is taken up in 500 ml of ether, washed twice with water and once with saturated sodium chloride solution, dried over sodium sulphate and the solvent removed. The residue is distilled under high vacuum until the last fraction passes over at 185° C. and 0.3 mbar. All distillates (44 g) are discarded. The distillation residue contains the product: brownish oil (144.7 g, 81%), which is reacted further without purification. Rf =0.25 (petroleum ether/ethyl acetate 10:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05032590
Source datasetuspto-grants-1991_07
ORD IDord-e2bd23c1acb14d04acb9dbdf3a9a86fe
Source noteuspto-grants-1991_07