Reaction #44480
ord-ef639e8403424da3a9b48ea36e8f9895
Reaction equation
N-(tert-butoxycarbonyl)-hexahydro-1H-azepin-4-one
O-benzylhydroxylamine hydrochloride
ammonium acetate
→
title compound
4-Amino-azepane-1-carboxylic acid tert-butyl ester
Reactants
Reagents
None
Solvents
Conditions
Detailed conditions
See reaction.notes.procedure_details.
Workup
- 1OtherThe solvent was evaporated in vacuo
- 2Otherthe crude oxime was purified by flash column chromatography (hexanes:ethyl acetate 100:0 to 50:50)
- 3workup.ADDITIONadded 10% by weight Pd/C (100 mg)
- 4FiltrationThe reaction was filtered through a pad of celite and filtrate
- 5Otherevaporated in vacuo
Procedure
A solution of N-(tert-butoxycarbonyl)-hexahydro-1H-azepin-4-one (0.5 g, 2.34 mmoles), O-benzylhydroxylamine hydrochloride (0.41 g, 2.57 mmoles) and ammonium acetate (0.45 g, 5.86 mmoles) in methanol (10 mL) was refluxed for 1.2 hours. The solvent was evaporated in vacuo and the crude oxime was purified by flash column chromatography (hexanes:ethyl acetate 100:0 to 50:50). The product was taken in 4N NH3 in methanol (10 mL) and added 10% by weight Pd/C (100 mg) and stirred over H2 at balloon pressure for twelve hours. The reaction was filtered through a pad of celite and filtrate evaporated in vacuo to provide the title compound.