HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 4-(5-Phenoxypentyl)benzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-(5-Phenoxypent-1-ynyl)benzyl alcohol | HCID 14576781 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(5-Phenoxypentyl)benzyl alcohol | HCID 14576782 | 99% |
Reaction Steps
4-(5-Phenoxypent-1-ynyl)benzyl alcohol--To a solution of 2.02 g of 4-5-phenoxypent-1-ynyl)benzaldehyde (from step (2) above) in 50 mL ethanol at 0° C. was added 640 mg sodium borohydride. After stirring for 1 hour, then addition of 8 mL water and evaporation of the solvents in vacuo, the residue was diluted with 2% H2SO4 and ethyl acetate. The organic layer was washed with brine and saturated NaHCO3 and then dried and the solvent evaporated in vacuo to give the title compound (99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05266713 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-3025a1c049d14277abbf116508c1d341 |
| Source note | uspto-grants-1993_11 |