HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Pentene, 5-bromo- → N-Benzylpent-4-en-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Pentene, 5-bromo- | HCID 70704 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,4-Dimethoxybenzylamine | HCID 597250 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-Benzylpent-4-en-1-amine | HCID 3839348 | 44% |
Reaction Steps
0.397 ml of 5-Bromo-1-pentene (3.35 mmol) and 0.67 ml of diisopropyl ethylamine (3.96 mmol) were added to the reaction solution containing 0.74 ml of benzylamine (a) (4.93 mmol) dissolved in acetonitrile with stirring and the mixture was stirred at room temperature for overnight. The reaction mixture was washed with saturated NaCl solution, dried over MgSO4, filtered and concentrated in vacuo. The resulting compound was purified with Silica gel column chromatography with EtOAc solvent as an eluant to give 236 mg of the pure title compound (b) (yield: 44%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07723376B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-b46ca452ea5c4dd981c162348aef3d32 |
| Source note | uspto-grants-2010_05 |