HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethylamine → N-(2-phenylethyl)but-3-en-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethylamine | HCID 1001 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Homoallyl bromide | HCID 21241 | — |
| Product | N-(2-phenylethyl)but-3-en-1-amine | HCID 16720109 | 62% |
Reaction Steps
To a solution of 2-phenylethylamine (72 mL, 570 mmol) is added K2CO3 (82 g, 570 mmol) and 4-bromo-1-butene (25 g, 185 mmol). The solution is stirred overnight at room temperature. The solution is evaporated to dryness and H2O/EtOAc (1:1) (600 mL) is added. The mixture is extracted with EtOAc (4×150 mL). The organic extracts are combined, dried and concentrated under vacuum. The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8) to provide 20 g (62%) of the title compound. M+H+=176.10.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08207183B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-4a6da6a3988b47f2a7ec0756122c8c30 |
| Source note | uspto-grants-2012_06 |