HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 1-(4-Fluorophenyl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2-(4-fluorophenyl)-1-phenylethanone | HCID 236329 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(4-Fluorophenyl)ethanol | HCID 73946 | — |
Reaction Steps
1-(4-Fluorophenyl)ethanol was prepared by mixing 10 g (72 mmol) of 4-fluorophenylacetophenone and 2.74 g (72 mmol) of sodium borohydride in 100 mL of ethanol. After one hour the solvent was removied under vacuum and the residue was taken up in diethyl ether. The ether solution was dried over anhydrous magnesium sulfate and evaporated to yield the crude product which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05026729 |
| Source dataset | uspto-grants-1991_06 |
| ORD ID | ord-9c54ec95f2104271b6c54f81db542827 |
| Source note | uspto-grants-1991_06 |