HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylbenzoyl Chloride → 4-methyl-N-(pyridin-4-ylmethyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylbenzoyl Chloride | HCID 13405 | — |
| Reactant | HCID 12797553 | HCID 12797553 | — |
| Product | 4-methyl-N-(pyridin-4-ylmethyl)benzamide | HCID 3117800 | 87.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04310532 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-174550f32a994a1091eeb0f103a619cb |
| Source note | uspto-grants-1982_01 |