HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 66783140, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 66783161 | HCID 66783161 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 66783140 | HCID 66783140 | 49.1% |
Reaction Steps
Sodium borohydride (59 mg, 1.6 mmol) was added at RT to a solution of 4-(tert-butyl-diphenyl-silanyloxy)-2-[3-methyl-2-oxo-4-(3-trifluoromethyl-phenyl)-piperazin-1-yl]-butyric acid methyl ester (480 mg, 0.78 mmol) in EtOH (7 mL), then after 20 h the reaction mixture was partitioned between 10% aq. KHSO4 solution and CH2Cl2. The organic layer was dried (MgSO4), filtered, and evaporated. Chromatography (SiO2; heptane/EtOAc 4:1) afforded the title compound (224 mg, 49%). Light yellow oil, MS: 585.4 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08138175B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-09722c1f69b84654b022b7903e014c79 |
| Source note | uspto-grants-2012_03 |