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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081213Generated: October 29, 2026

AcOH AcOAc → HCID 23366109, compound

https://huagongshe.com/reaction/1081213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcOH AcOAcHCID 21895370—
ReactantHCID 85194979HCID 85194979—
CatalystNickelHCID 935—
ProductHCID 23366109HCID 2336610949%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05583221
Source datasetuspto-grants-1996_12
ORD IDord-b5daaa2aa3604d87a5c58cba8f22c9cd
Source noteuspto-grants-1996_12