HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 69891916, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (1R*,5S*,6R*)-8-Benzyl-6-(tert-butoxycarbonyl)-1-phenyl-8-azabicyclo[3.2.1]octan-2-one | HCID 69889518 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 69891916 | HCID 69891916 | — |
Reaction Steps
Sodium borohydride (8.7 g, 0.23 mol) was added to a stirred suspension of (1R*,5S*,6R*)-8-benzyl-6-(tert-butoxycarbonyl)-1-phenyl-8-azabicyclo[3.2.1]octan-2-one (Description 19a; 76 g, 0.23 mol) in methanol (700 ml) at room temperature. The reaction mixture was stirred overnight, quenched with water and concentrated in vacuo. The residue was extracted into ethyl acetate. The combined organic extracts were dried (MgSO4) and concentrated in vacuo to give the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06727249B2 |
| Source dataset | uspto-grants-2004_04 |
| ORD ID | ord-4da6a0903373461b86c4f77e2cfa8744 |
| Source note | uspto-grants-2004_04 |