HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 57951159, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 57951114 | HCID 57951114 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57951159 | HCID 57951159 | 67% |
Reaction Steps
Stir 4-(3-fluoro-phenyl)-N-(4-trifluoromethoxy-phenyl)-4-oxo-butyramide (3.0 g, 8.5 mmol) in ethanol (70 mL) at room temperature. Add sodium borohydride (650 mg, 17.2 mmol) portionwise and stir at room temperature until TLC indicates that no starting material remains. Add acetone to quench excess borohydride, concentrate the reaction mixture under reduced pressure, redissolve in ethyl acetate and wash with brine. Dry over anhydrous magnesium sulfate, evaporate under reduced pressure to give the titled compound (2.0 g, 67% yield) MS (m/z): 358(M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08168659B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-4e2af5c27e4042378e0bcf888c2fab39 |
| Source note | uspto-grants-2012_05 |