HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 53640764, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 21186660 | HCID 21186660 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 53640764 | HCID 53640764 | 31.3% |
Reaction Steps
A mixture of sodium borohydride (0.090 g, 2.38 mmol) and ethanol (5 mL) was stirred 10 min and then 1-(3,5-dimethyl-4-triisopropylsilyloxyphenyl)-2-(4-(4-trifluoromethylphenyl)-4-hydroxypiperidin-1-yl)-propan-1-one (1.30 g, 2.25 mmol in 25 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 0.408 g (31%) of (1R*,2R*)-1-(3,5-dimethyl-4-triisopropylsilyloxyphenyl)-2-(4-(4-trifluoromethylphenyl)-4-hydroxypiperidin-1-yl)-propan-1-ol which was suitable for use without further purification and had: mp 177-177.5° C. Analysis calculated for C32H48F3NO3Si.0.25 H2O: C, 65.78; H, 8.37; N, 2.40. Found: C, 65.65; H, 8.51; N, 2.57.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06046213 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-44d8af16ac974090a40b86007c9cf2b8 |
| Source note | uspto-grants-2000_04 |