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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432782Generated: October 31, 2026

4-Pyridinecarboxaldehyde → HCID 68702352, compound

https://huagongshe.com/reaction/432782

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PyridinecarboxaldehydeHCID 13389—
ReactantSodium HydroxideHCID 14798—
Reactant1-Methyl-4-piperidoneHCID 74049—
CatalystHexadecyltrimethylammonium chlorideHCID 8154—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 68702352HCID 68702352182%

Reaction Steps

To a solution of 1.0 g (8.84 mmol) of 1-methylpiperidine-4-one and 1.89 g (16.70 mmol) of 4-pyridine carboxaldehyde in 88 mL of a 0.25M solution of aqueous NaOH (22.09 mmol) was added 1.16 mL (0.88 mmol) of a 25% w/w aqueous solution of cetyltrimethylammonium chloride. The mixture was allowed to stir vigorously at room temperature for 3 hours, diluted with 100 ml of brine and extracted with two 60 mL portions of methylene chloride. The organic phase was dried over anhydrous MgSO4 and concentrated in vacuo to give 2.15 g (84%) of a yellow-orange powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06664272B2
Source datasetuspto-grants-2003_12
ORD IDord-2179dfe2f8cc4bf293842ce575349435
Source noteuspto-grants-2003_12