HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Benzyloxy)benzaldehyde → Benzenemethanol, 2-(phenylmethoxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Benzyloxy)benzaldehyde | HCID 344784 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium borohydride | HCID 4311764 | — |
| Product | Benzenemethanol, 2-(phenylmethoxy)- | HCID 18811 | — |
Reaction Steps
To a stirring solution of 2-(benzyloxy)benzaldehyde (10 g, 47 mmol) in 100 mL of Ethanol, NaBH4 was added as a solid in small portions. The reaction temperature was controlled with a room temperature water bath. After stirring for 30 minutes, the reaction was quenched by slow addition of 3N HCl. This solution was extracted with EtOAc and the organic portion washed with water, Sat. Na2CO3 and brine. The solution was dried (Na2SO4), filtered, and concentrated in vacuo to provide the benzy alcohol which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329376B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-3abbb2c502914ae0b68a27d93d3b03b8 |
| Source note | uspto-grants-2001_12 |