HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(4-Bromophenyl)propionic acid → 3-(4-Bromophenyl)propan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(4-Bromophenyl)propionic acid | HCID 2735609 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(4-Bromophenyl)propan-1-ol | HCID 10560614 | — |
Reaction Steps
To a solution of 3-(4-bromo-phenyl)-propionic acid (4.0 g, 18 mmol) in THF (30 mL) at 0° C. under the argon atmosphere was added LiAlH4 (1.0 M in THF; 14 mL, 14 mmol). After the addition, the ice-bath was removed and the mixture refluxed for 18 h. After cooling to room temperature, the reaction was quenched with 1 M HCl and the mixture extracted with ethyl acetate. The organic layer was separated, washed with brine, dried over Na2SO4 and filtered. The filtrate was concentrated and the crude product used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08030487B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-7bfdf2391f214c3c9f65169fc0a92927 |
| Source note | uspto-grants-2011_10 |