Hydroxyamine hydrochloride → HCID 68294859, compound
Reaction equation
C[O:2][C:3]1(OC)[CH2:9][CH2:8][CH2:7][CH2:6][CH:5]([C:10](=[O:16])[C:11]([O:13][CH2:14][CH3:15])=[O:12])[C:4]1=O.Cl.[NH2:21]O>CCO>[O:2]=[C:3]1[C:4]2=[N:21][O:16][C:10]([C:11]([O:13][CH2:14][CH3:15])=[O:12])=[C:5]2[CH2:6][CH2:7][CH2:8][CH2:9]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of ethyl (3,3-dimethoxy-2-oxocycloheptyl)(oxo)acetate (0.850 g, 3.12 mmol) in 15 mL of EtOH, hydroxylamine hydrochloride (0.225 g, 3.24 mmol) was added. The mixture was stirred at room temperature overnight. The solvent was removed under reduced pressure and the crude solid was purified by flash chromatography on silica gel (eluant: AcOEt/hexane:1/9) to afford 0.245 g (35% yield) of:
Workup
- customThe solvent was removed under reduced pressure
- customthe crude solid was purified by flash chromatography on silica gel (eluant: AcOEt/hexane:1/9)
- customto afford 0.245 g (35% yield) of:
Sources & evidence
- ORD record
- ord-fc95ef0a762c4f848958838da7431798
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08916577B2
Reaction notes
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