HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylbenzaldehyde → Pyridinium, 1-methyl-, tetraphenylborate(1-) (1:1)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylbenzaldehyde | HCID 7725 | — |
| Reactant | HCID 13865068 | HCID 13865068 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Pyridinium, 1-methyl-, tetraphenylborate(1-) (1:1) | HCID 11090946 | 78% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05912257 |
| Source dataset | uspto-grants-1999_06 |
| ORD ID | ord-29f9c4eda57242ae881c1d4b03d992c8 |
| Source note | uspto-grants-1999_06 |