Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Acetone Cyanohydrin | HCID 6406 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | 4-Benzyl-4-piperidinol | HCID 98152 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 17956592 | HCID 17956592 | — |
Reaction Steps
To a suspension of 4-benzyl-piperidin-4-ol (1.0 g, 5.2 mmol), benzaldehyde (0.83 g, 7.8 mmol) and MgSO4 (0.31 g, 2.6 mmol) in 1-methyl-2-pyrrolidone (5 mL) is added acetone cyanohydrine (0.45 g, 5.2 mmol). The reaction mixture is heated at 50° C. for 2 h, then cooled to room temperature and quenched with ice (20 g) and sat. NaHCO3 (50 mL). The aqueous phase is extracted with Et2O (3×100 mL), the combined organic extracts are washed with sat. NaCl (20 mL), dried (Na2SO4), filtered and evaporated. The residue is dissolved in THF (20 mL) and added to a suspension of LiAlH4 (1.1 g, 27.6 mmol) in THF (80 mL) at 0° C. The reaction mixture is stirred for 15 h at room temperature and quenched with EtOAc (250 mL), MeOH (20 mL) and sat. NaHCO3 (5 mL). The precipitate is filtered off, washed with MeOH (20 mL) and the filtrate evaporated. Purification by preparative HPLC provides the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07375227B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-318cc3a9954542c4bd222663c520cbbb |
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| Source note | uspto-grants-2008_05 |
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