HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrobenzyl alcohol → 4-Aminobenzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrobenzyl alcohol | HCID 69275 | — |
| Reactant | CID 24201897 | HCID 24201897 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Aminobenzyl alcohol | HCID 69331 | 35.5% |
Reaction Steps
To a solution of 4-nitrobenzylalcohol (4.59 g) in methanol (300 ml) was added copper chloride (I) (17.8 g) at room temperature, and then was gradually added potassium boron hydride (11.3 g) for 40 minutes. The reaction mixture was stirred at room temperature for 2 hours and concentrated under reduced pressure. To the residue was added water, and the mixture was extracted with ethyl acetate. The organic layer was dried with anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was separated and purified with column chromatography (ethyl acetate/hexane=3/1) to give 4-aminobenzylalcohol (1.31 g) as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06172061B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-114a7bab729348a886dee4de7d4ec93b |
| Source note | uspto-grants-2001_01 |