HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 14521578, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 14521576 | HCID 14521576 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 14521578 | HCID 14521578 | — |
Reaction Steps
NaBH4 (2.56 g, 67.7 mmol) was added to a solution of 2-carbomethoxy-8-oxabicyclo(3.2.1)octan-3-one, 3, (5.12 g, 27.8 mmol) in MeOH (100 mL) at −78° C. The reaction mixture was left at room temperature overnight. The solution was concentrated to dryness. The residue was dissolved in water (50 mL), and extracted with CH2Cl2 (100, 2×50 mL). The combined dried (MgSO4) extracts were concentrated to dryness (yield: 3.9 g). By repeated flash column chromatography four isomers were obtained from the residue (2.9 g). The major isomer was 2α-carbomethoxy-3α-hydroxy-8-oxabicyclo(3.2.1)octane (1.0 g, 26%). Some of the other isomers were isolated to be used in the following reactions but there were still mixed fractions. Other pure isomers obtained:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06670375B2 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-87f9909b49b74e168b3e99965564caef |
| Source note | uspto-grants-2003_12 |