HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propargyl bromide → N-(4-Chlorobenzyl)-N-methyl-2-propinylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzenemethanamine, 4-chloro-N-methyl- | HCID 66905 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-(4-Chlorobenzyl)-N-methyl-2-propinylamine | HCID 60670247 | — |
Reaction Steps
To a solution of 31.1 g (0.2 mole) N-(4-chlorobenzyl)-methylamine and 30.3 g (0.3 mole) triethylamine in 150 ml dry benzene are added in portions at room temperature while stirring 23.8 g (0.2 mole) propargyl bromide. The solution is heated for 17 hours with reflux. After filtering off the solid phase, the the solvent is distilled under vacuum and the remaining residue fractionally distilled under reduced pressure. One thus obtains 30.9 g N-(4-chlorobenzyl)-N-methyl-2-propinylamine (79% of the theory as colorless liquid of the boiling point 86°-106° C./2 Torr.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04156017 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-93afa677ad014a24897f6c7cb1ad684e |
| Source note | uspto-grants-1979_05 |