Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1105792Generated: November 1, 2026

4-Methylbenzoyl Chloride → 4-methyl-N-(pyridin-4-ylmethyl)benzamide

https://huagongshe.com/reaction/1105792

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methylbenzoyl ChlorideHCID 13405—
ReactantHCID 12797553HCID 12797553—
Product4-methyl-N-(pyridin-4-ylmethyl)benzamideHCID 311780087.7%

Reaction Steps

N-(4-pyridylmethyl)-p-methylbenzamide was synthesized from p-toluoyl chloride and 4-pryidylmethylamine in the same manner as employed in Example 1 above. The pure product has a melting point 142.7° C., yield of 87.7%. The intermediate product was converted to pure N-(4-piperidinylmethyl)-p-methylbenzamide as previously described (Example 1); melting point 226.6° C., yield 70.7%, and evaluated according to Tables I, II, and III.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04310532
Source datasetuspto-grants-1982_01
ORD IDord-174550f32a994a1091eeb0f103a619cb
Source noteuspto-grants-1982_01