Hydrochloric Acid → HCID 19968452, compound
Reaction equation
[O:1]=[C:2]1[C:7]2([CH2:11][CH2:10][CH2:9][CH2:8]2)[NH:6][CH2:5][CH2:4][CH:3]1C(OCC)=O.Cl>O>[CH2:11]1[C:7]2([C:2](=[O:1])[CH2:3][CH2:4][CH2:5][NH:6]2)[CH2:8][CH2:9][CH2:10]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of ethyl 10-oxo-6-azaspiro[4.5]decan-9-carboxylate (7.6 g), concentrated hydrochloric acid (35 ml) and water (35 ml) was heated at 90°-95° C. for 8 hours. The solvent was removed in vacuo and the residue diluted with ice-water (35 ml) and basified by the addition of an excess of 5M aqueous sodium hydroxide solution. The product was extracted into ethyl acetate and the extracts were washed with brine, dried over magnesium sulphate and the solvent removed in vacuo to give 6-azaspiro[4.5]decan-10-one. Yield 3.1 g.
Workup
- temperaturewas heated at 90°-95° C. for 8 hours
- customThe solvent was removed in vacuo
- additionthe residue diluted with ice-water (35 ml)
- additionbasified by the addition of an excess of 5M aqueous sodium hydroxide solution
- extractionThe product was extracted into ethyl acetate
- washthe extracts were washed with brine
- dry with materialdried over magnesium sulphate
- customthe solvent removed in vacuo
Sources & evidence
- ORD record
- ord-36e9b44e73754e6aa3e5f18f3b61fcff
- Source dataset
- uspto-grants-1997_03
- Patent number
- US05610161
Reaction notes
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