Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | AcOH AcOAc | HCID 21895370 | — |
| Reactant | HCID 85194979 | HCID 85194979 | — |
| Catalyst | Nickel | HCID 935 | — |
| Product | HCID 23366109 | HCID 23366109 | 49% |
Reaction Steps
A solution of 8-methyl-8-azabicyclo[3.2.1]octane-2,3-dione-2-oxime (0.93 g, 5.5 mmol) in acetic acid/acetic anhydride (4:1, 40 mL) in a Parr bottle was treated with Raney nickel (Aldrich, 1/2 tsp.), then subjected to hydrogenation in a Parr apparatus at 45-50 psi for 5 h The solution was carefully evacuated of hydrogen, filtered through Celite® (wash filter cake carefully with methanol), and the filtrate was concentrated in vacuo. The residue was taken up in toluene and reconcentrated to remove most of the acetic acid. This residue was taken up in saturated sodium carbonate (40 mL), then treated with 15% sodium hydroxide (2 mL) and extracted with methylene chloride (3×50 mL) containing some 2-propanol. The combined extracts were dried (Na2SO4), concentrated in vacuo, and chromatographed on silica gel (eluted with 1:1 ethyl acetate/methanol) to afford a white solid, which contained some silica gel. This was removed by dissolving the product in warm ethyl acetate, filtering, and concentration in vacuo to afford 2-acetamido-8-methyl-8-azabicyclo[3.2.1]octan-3-one (0.53 g, 49%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05583221 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-b5daaa2aa3604d87a5c58cba8f22c9cd |
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| Source note | uspto-grants-1996_12 |
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