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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487474Generated: October 28, 2026

Formaldehyde → 2-(1-Acetylpiperidin-4-yl)propenal

https://huagongshe.com/reaction/487474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantDimethylazanium;chlorideHCID 12954980—
ReactantEthanone,1-[4-(2-hydroxyethyl)-1-piperidinyl]-HCID 21468226—
Product2-(1-Acetylpiperidin-4-yl)propenalHCID 45119214—

Reaction Steps

3.95 g (23.3 mmol) of 2-(1-acetylpiperidin-4-yl)ethanol, 2.12 g (26.3 mmol) of dimethylammonium chloride and 3 ml (40 mmol) of 37% formaldehyde solution are heated at 110° C. for 2 hours with stirring. The mixture is allowed to cool and is extracted several times with diethyl ether. The organic phases are combined, washed with saturated sodium chloride solution, dried over sodium sulfate, filtered and concentrated to dryness by evaporation. 2-(1-acetylpiperidin-4-yl)propenal is obtained in the form of a yellowish oil which can be further reacted without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05294734
Source datasetuspto-grants-1994_03
ORD IDord-604b3f2eec244a168750a5e227725d99
Source noteuspto-grants-1994_03