HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → 4-[3-(2-Hydroxyethylamino)propyl]benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(3-Bromopropyl)benzonitrile | HCID 458364 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-[3-(2-Hydroxyethylamino)propyl]benzonitrile | HCID 69071579 | 57.6% |
Reaction Steps
To a solution 4-(3-bromopropyl)benzonitrile (8 g, 0.0357 mol; see step (iv) above) in dry acetonitrile (150 mL) were added anhydrous K2CO3 (7.4 g, 0.0535 mol) and ethanolamine (10.9 g, 0.179 mol). The resulting reaction mixture was then stirred overnight at room temperature, after which it was filtered and concentrated. The crude product thus obtained was purified by column chromatography over silica gel, using methanol in chloroform as eluent, to yield 4.2 g (57.5%) of the sub-title compound as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07354917B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-3d440c14301246ca95306f3c3a98cce4 |
| Source note | uspto-grants-2008_04 |