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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185577Generated: October 31, 2026

4-Methylbenzaldehyde → Pyridinium, 1-methyl-, tetraphenylborate(1-) (1:1)

https://huagongshe.com/reaction/2185577

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylbenzaldehydeHCID 7725—
ReactantHCID 13865068HCID 13865068—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
ProductPyridinium, 1-methyl-, tetraphenylborate(1-) (1:1)HCID 1109094678%

Reaction Steps

In a 500-mL one-neck flask fitted with a stirrer and a condenser, 1.2 g (0.01 mol) of 4-methylbenzaldehyde, 0.01 mol of 4-methyl-N-methylpyridinium tetraphenylborate, and 30 mL of absolute ethanol were mixed. Five drops of piperidine was added to the mixture. The solution was then heated to reflux, refluxed overnight, cooled, and filtered. The collected solid was washed twice with ether and twice with water to obtain 4-[p-N-methyl-N-ethylamino)styryl]-N-methylpyridinium tetraphenylborate in 78% yield as a reddish solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06402037B1
Source datasetuspto-grants-2002_06
ORD IDord-da59c83da15d4c6592f2c999b7403f72
Source noteuspto-grants-2002_06