HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384299Generated: October 31, 2026
Sodium borohydride → HCID 15453440, compound
https://huagongshe.com/reaction/1384299
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 15453439 | HCID 15453439 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 15453440 | HCID 15453440 | — |
Reaction Steps
A mixture of sodium borohydride (0.027 g, 0.717 mmol) and ethanol (10 mL) was stirred 10 min and then 1-(3-fluoro-4-triisopropylsilyloxyphenyl)-2-(4-(4-fluorophenyl)-4-hydroxypiperidin-1-yl)-propan-1-one (0.371 g, 0.717 mmol in 10 mL of ethanol) was added. The reaction was stirred at ambient temperature overnight. The mixture was concentrated and the residue was partitioned between ethyl acetate and water. The phases were separated and the organic phase was washed with brine, dried over calcium sulfate and concentrated. The residue was flash chromatographed on silica gel (0.75×3 inches packed in hexane) with elution proceeding as follows: 10% ethyl acetate/hexane (200 mL), nil; 10% ethyl acetate/hexane (100 mL) and 20% ethyl acetate/hexane (200 mL), to give 0.22 g (59%) of (1R*, 2R*)-1-(3-fluoro-4-triisopropylsilyloxyphenyl)-2-(4-(4-fluorophenyl)-4-hydroxypiperidin-1-yl)-propan-1-ol. A sample recrystallized from ether had: mp 159-160° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06258827B1 |
|---|
| Source dataset | uspto-grants-2001_07 |
|---|
| ORD ID | ord-dae04e8dedf345ee91b564119e29867b |
|---|
| Source note | uspto-grants-2001_07 |
|---|