HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → Benzyl 3-(hydroxymethyl)-8-azabicyclo[3.2.1]octane-8-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Benzyl 3-formyl-8-azabicyclo[3.2.1]octane-8-carboxylate | HCID 51030438 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzyl 3-(hydroxymethyl)-8-azabicyclo[3.2.1]octane-8-carboxylate | HCID 53487624 | — |
Reaction Steps
To a solution of EXAMPLE 84B (3.4 g) in tetrahydrofuran (40 mL) was added NaBH4 (0.5 g). The mixture was stirred overnight. The solvent was evaporated and the residue was added to ethyl acetate (300 mL) and water (50 mL). The organic layer was washed with water and brine, dried over Na2SO4, and filtered. Evaporation of the solvent gave the crude title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09227963B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-df906687936442bc9e386de493fb6846 |
| Source note | uspto-grants-2016_01 |