HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Phenylcyclohexanone → 4-Phenylcyclohexanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Phenylcyclohexanone | HCID 78605 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Phenylcyclohexanol | HCID 79497 | 66.2% |
Reaction Steps
To a solution of 31.4 g (0.18 mol) of 4-phenylcyclohexanone in 500 ml of absolute methanol, which is cooled to -10° C., are added 6.8 g (0.18 mol) of sodium borohydride in batches with stirring. The reaction mixture is allowed to react for 0.5 hours at -10° C. and for 3 hours at ambient temperature and then evaporated down in vacuo. The residue remaining is mixed with water and acidified with 2N hydrochloric acid. The suspension formed is stirred for 1 hour and the crystalline product is suction filtered, dried and recrystallised from diisopropylether. 21 g (66% of theory) of 4-phenylcyclohexanol are obtained, melting point: 112°-114° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05726205 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-59ad5f10a39944bab640d9fbd6671548 |
| Source note | uspto-grants-1998_03 |