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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613873Generated: October 26, 2026

Formaldehyde → 5-(2-Piperidinomethylbutyryl)-3-phenylisoxazole

https://huagongshe.com/reaction/1613873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantPiperidineHCID 8082—
Reactant3-Phenyl-5-butyrylisoxazoleHCID 10130602—
SolventEthanolHCID 702—
Product5-(2-Piperidinomethylbutyryl)-3-phenylisoxazoleHCID 11758777—

Reaction Steps

Added to 320 ml of ethyl alcohol were 160 g (0.74 mol) of 5-butyry-3-phenylisoxazole and 103 ml of piperidine, followed by the dropwise addition of 96 ml (1.18 mol) of a 37% aqueous solution of formaldehyde under ice cooling over 30 minutes. After the reaction mixture was stirred for 1.5 hours at room temperature, the solvent was distilled off. The residue was dissolved in 800 ml of ethyl ether. The resultant solution was washed with water and the organic layer then dried over anhydrous magnesium sulfate. The solvent was distilled off, whereby the target compound, 5-(2-piperidinomethylbutyryl)-3-phenylisoxazole was obtained as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05194606
Source datasetuspto-grants-1993_03
ORD IDord-1c764e0433df48c9b06c648d620e6e07
Source noteuspto-grants-1993_03