HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 3-(Aminomethyl)-1-benzylpiperidin-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | (Dimethyl sulfide)trihydroboron | HCID 12423031 | — |
| Reactant | HCID 68684193 | HCID 68684193 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(Aminomethyl)-1-benzylpiperidin-4-ol | HCID 23003732 | 51% |
Reaction Steps
A suspension of 4-hydroxy-1-(phenylmethyl)-3-piperidinecarboxamide (5.62 g, 23.9 mmol) in THF (65 mL) was treated dropwise with borane-methyl sulphide complex (2M solution in THF, 26.4 mL, 52.8 mmol). After stirring for 0.5 h at room temperature, the reaction mixture was heated at 80° C. for 1.5 h. Methanol (16 mL) was added and heating continued for 0.5 h. The mixture was evaporated and the residue was chromatographed on silica gel, eluting with 10-30% (2M ammonia/methanol)/dichloromethane to give the product (2.67 g, 51%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08071592B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-2a805150c29f4d3598fcd09386911c3a |
| Source note | uspto-grants-2011_12 |