HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 19848717, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 12281017 | HCID 12281017 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19848717 | HCID 19848717 | — |
Reaction Steps
A solution of ethyl 4-oxo-1-azabicyclo[3.3.1]non-3-yl carboxylate* (22 g, 0.104 moles) in ethanol (200 ml) was cooled in an ice bath to 5° C. and treated portionwise with sodium borohydride (4.0 g). The reaction was then allowed to warm to room temperature and stirred overnight. The solvent was then removed in vacuo, the residue partitioned between dichloromethane (200 ml) and water (75 ml) and the organic layer separated and dried (Na2SO4). Filtration and removal of the solvent afforded the required product as an oil (20.0 g), 85% pure by g.l.c. (OVl, 180° C.) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04870081 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-341f34e8947641668fb2998d4bdf62ad |
| Source note | uspto-grants-1989_09 |