HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethyl bromide → N,N-Dimethylphenylethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N,N-Dimethylphenylethylamine | HCID 25125 | — |
Reaction Steps
2-Phenylethyl bromide [0.01 mol.] and dimethylamine hydrochloride [0.02 mol.] are stirred at room temperature [24 hrs] and then refluxed [1 hr.] with potassium carbonate [0.06 in methanol. The insoluble materials are filtered and the solution evaporated and distilled to form N,N-dimethyl-2-phenylethylamine. The hydrochloride salt [m.p. 163-4° C.] is formed and recrystallized from ethanol. The structure was confirmed by its proton nmr spectrum, by its chemical ionization mass spectrum, and its correct elemental analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05322859 |
| Source dataset | uspto-grants-1994_06 |
| ORD ID | ord-20846a74e371493caea3044c10c341a7 |
| Source note | uspto-grants-1994_06 |