HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 59598495, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 59598486 | HCID 59598486 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 59598495 | HCID 59598495 | 139.3% |
Reaction Steps
To a solution of (R)-tert-butyl 3-(6-fluoro-3′-methylbiphenylcarbonyl)piperidine-1-carboxylate (3.5 g, 6.29 mmol) in MeOH (50 mL) was added NaBH4 (0.95 g, 25 mmol) in portions at rt. After addition, the mixture was stirred for 2 h. Tlc showed the starting material had disappeared. The solvent was removed in vacuo to leave a residue which was partitioned between water and EtOAc. The organic layer was washed with H2O and brine, dried over Na2SO4 and evaporated to give (3R)-tert-butyl 3-((6-fluoro-3′-methylbiphenyl-2-yl)(hydroxy)methyl)piperidine-1-carboxylate (3.5 g, 100%), which was used in the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07858624B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-de4b5d46774d47228995b78f6dba8e3a |
| Source note | uspto-grants-2010_12 |