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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613872Generated: October 27, 2026

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

https://huagongshe.com/reaction/1613872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantPiperidineHCID 8082—
Reactant5-Propionyl-3-phenylisoxazoleHCID 15180766—
SolventEthanolHCID 702—
Product5-(2-Piperidinomethylpropionyl)-3-phenylisoxazoleHCID 15227816—

Reaction Steps

Added to 10 ml of ethyl alcohol were 2.0 g (10.0 mmol) of 5-propiony-3-phenylisoxazole and 1.7 g (20.0 mmol) of piperidine, followed by the dropwise addition of 1.63 ml (20.0 mmol) of a 37% aqueous solution of formaldehyde under ice cooling. After the reaction mixture was stirred for 2 hours at room temperature, the solvent was distilled off under reduced pressure. The residue was dissolved in ethyl ether. The organic layer was washed with water and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, whereby the target compound, namely, 5-(2-piperidinomethylpropionyl)-3-phenylisoxazole was obtained as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05194606
Source datasetuspto-grants-1993_03
ORD IDord-64c6837c7545443e8adac51e118aeb57
Source noteuspto-grants-1993_03