HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → N-[(4-Chlorophenyl)methyl]-N-methylacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Diketene | HCID 12661 | — |
| Reactant | Benzenemethanamine, 4-chloro-N-methyl- | HCID 66905 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-[(4-Chlorophenyl)methyl]-N-methylacetamide | HCID 12633526 | — |
Reaction Steps
Dissolved in toluene was 3.1 g (0.02 mole) of 4-chloro-N-methyl-benzylamine, followed by an addition of a catalytic amount of pyridine and a further dropwise addition of 1.8 g (0.022 mole) of diketene at room temperature. After stirring the reaction mixture at room temperature for 3 hours, it was poured in water and then extracted with toluene. Subsequent to purification, N-methyl-N-(4-chlorobenzyl)acetamide was obtained in an oily form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04736038 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-24ea25f346d941ba906ebffb01c3eb53 |
| Source note | uspto-grants-1988_04 |