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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073096Generated: November 3, 2026

Acetic Acid → HCID 54092388, compound

https://huagongshe.com/reaction/1073096

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968681
Source datasetuspto-grants-1990_11
ORD IDord-57d12dbe4ecd4454b9eed05df956edf1
Source noteuspto-grants-1990_11