HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 1-Phenylcyclohexanemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-Phenylcyclohexane-1-carbaldehyde | HCID 14922606 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Phenylcyclohexanemethanol | HCID 198517 | 91.7% |
Reaction Steps
To a stirred solution of 1-phenyl-cyclohexanecarbaldehyde (250) (16.4 g, 87.1 mmol) in methanol (200.0 mL) was added NaBH4 (6.62 g, 174.2 mmol) portion-wise at 0° C. The reaction mixture was then stirred at room temperature for 2 h. After completion of the reaction, the solvent was concentrated and the crude product was extracted with ethyl acetate. The organic layer was then washed with water and brine and dried over sodium sulfate and concentrated under reduced pressure to get (1-phenyl-cyclohexyl)-methanol (251) (15.2 g, 91.7%) as a white solid which was sufficiently pure to be used for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09045486B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-66f33b7649ef455c9f5dea3a4d18ecd7 |
| Source note | uspto-grants-2015_06 |