HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium borohydride → HCID 59577304, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 59577252 | HCID 59577252 | — |
| Product | HCID 59577304 | HCID 59577304 | 24.7% |
Reaction Steps
Benzyl 3-[4-(2-tert-butylphenoxy)piperidin-1-yl]-3-oxo-2-phenylpropanoate (167 mg, 0.34 mmol) obtained in Example 174 and lithium tetrahydroborate (2.0M, THF solution, 0.41 mL, 0.82 mmol) were stirred at room temperature for 3 days. The reaction mixture was partitioned between ethyl acetate and saturated aqueous ammonium chloride, and the ethyl acetate layer was dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate 75:25-25:75) to give the title compound (32 mg, 24%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08586571B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-bf603a0fdd0e48d78f23abfd899e2143 |
| Source note | uspto-grants-2013_11 |