HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 54480353, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 21186659 | HCID 21186659 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 54480353 | HCID 54480353 | 65% |
Reaction Steps
A mixture of sodium borohydride (0.085 g, 2.25 mmol) and ethanol (5 mL) was stirred 10 min and then 1-(4-benzyloxy-3,5-difluorophenyl)-2-(4-(4-trifluoromethylphenyl)-4-hydroxypiperidin-1-yl)-propan-1-one (1.02 g, 1.96 mmol in 30 mL of ethanol) was added. The reaction was stirred at ambient temperature overnight. The white solid which precipitated was collected by filtration and dried to yield 0.66 g (65%) of (1R*,2R*)-1-(4-benzyloxy-3,5-difluorophenyl)-2-(4-(4-trifluormethylphenyl)-4-hydroxypiperidin-1-yl)-propan-1-ol which was suitable for use without further purification and had: mp 201-202° C. Analysis calculated for C28H28F5NO3.0.25 H2O: C, 63.93; H, 5.46; N, 2.66. Found: C, 63.98; H, 5.49; N, 2.70.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06046213 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-374cc261f0f145ff96cbd81786fb7a3d |
| Source note | uspto-grants-2000_04 |