HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 4-(p-Fluorophenyl)-3-cyclohexen-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22610268 | HCID 22610268 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(p-Fluorophenyl)-3-cyclohexen-1-ol | HCID 21534465 | 96% |
Reaction Steps
A solution of 0.065 mole of 4-(p-fluorophenyl)-3-cyclohexen-1-one (obtained as in Example 7) and 6 g. of sodium borohydride in 130 ml. of ethanol is stirred at room temperature for about 5 hours. The bulk of the solvent is removed on a rotary evaporator and the residue diluted with water. The precipitated solid is collected on a filter and recrystallized from Skellysolve B to give a 96% yield of 4-(p-fluorophenyl)-3-cyclohexen-1-ol having a melting point of 73° to 74.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03960961 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-9c2bafb466cb476e89c4de00865d83b5 |
| Source note | uspto-grants-1976_06 |