HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 70235707, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 21186595 | HCID 21186595 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 70235707 | HCID 70235707 | 57% |
Reaction Steps
A mixture of sodium borohydride (0.058 g, 1.40 mmol) and ethanol (5 mL) was stirred 10 min and then 1-(3,5-difluoro-4-triisopropylsilyloxyphenyl)-2-(4-(-4-chlorophenyl)-4-hydroxypiperidin-1-yl)-propan-1-one (0.76 g, 1.38 mmol in 20 mL of ethanol) was added. The reaction was stirred at ambient temperature over the weekend. The white solid which precipitated was collected by filtration and dried to yield 0.43 g (57%) of (1R*,2R*)-1-(3,5-difluoro-4-triisopropylsilyloxyphenyl)-2-(4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl)-propan-1-ol which was suitable for use without further purification and had: mp 192-192.5° C. Analysis calculated for C29H42ClF2NO3Si.0.25 H2O: C, 62.35; H, 7.67; N, 2.51. Found: C, 62.37; H, 7.81; N, 2.73.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06258827B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-004047694c3c4adfa7ac825ae32f0fe4 |
| Source note | uspto-grants-2001_07 |