HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 1-(4-Amino-3'-fluoro[1,1'-biphenyl]-3-yl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ammonium Sulfate | HCID 6097028 | — |
| Reactant | 1-(4-Amino-3'-fluoro[1,1'-biphenyl]-3-yl)ethanone | HCID 22021891 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(4-Amino-3'-fluoro[1,1'-biphenyl]-3-yl)ethanol | HCID 22021899 | 67% |
Reaction Steps
A solution of 1-(4-amino-3′-fluoro[1,1′-biphenyl]-3-yl)ethanone (3 g, 13 mmol) in anhydrous methanol (60 mL) was treated at rt under nitrogen with sodium borohydride in a portion wise manner. After addition, the reaction mixture was stirred for 4 hours, treated with a saturated aqueous ammonium sulfate solution (50 mL) and ethyl acetate (100 mL). The organic layer was separated, dried (MgSO4) and evaporated. The residue was purified on a silica gel column chromatography (hexane:ethyl acetate/3:1) to yield 1-(4-amino-3′-fluoro[1,1′-biphenyl]-3-yl)ethanol as a white solid (2 g, 67%): mp 136-137° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06713478B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-f4797b5fcdf04f7aa4a77f4ea31c165e |
| Source note | uspto-grants-2004_03 |