HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(4-Aminophenyl)propionic acid → 4-Aminobenzenepropanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(4-Aminophenyl)propionic acid | HCID 75451 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Product | 4-Aminobenzenepropanol | HCID 220424 | 89% |
Reaction Steps
To a mixture of 3-(4-amino-phenyl)-propionic acid (1.85 g, 11.2 mmol) and tetrahydrofuran′(200 ml), was added lithium aluminum hydride (1.0 g, 26 mmol). After stirring for 3 hours, the mixture was quenched by addition of methanol (5 ml) and concentrated under reduced pressure. The residue was treated with saturated aqueous sodium chloride solution (100 ml) and extracted with ethyl acetate (200 ml). The organic extract was concentrated under reduced pressure to give 3-(4-amino-phenyl)-propan-1-ol (1.5 g, 89% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07419984B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-2d30637f3a09471486294a64214e35e3 |
| Source note | uspto-grants-2008_09 |