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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416340Generated: October 30, 2026

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

https://huagongshe.com/reaction/1416340

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 numberUS05912257
Source datasetuspto-grants-1999_06
ORD IDord-29f9c4eda57242ae881c1d4b03d992c8
Source noteuspto-grants-1999_06