Hydroxyamine hydrochloride → HCID 136408146, compound
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([C:12]([CH3:15])([CH3:14])[CH3:13])[C:5]([OH:11])=[C:6]([C:8](=O)[CH3:9])[CH:7]=1.CC([O-])=O.[Na+].[NH2:21][OH:22].Cl>CCO>[Br:1][C:2]1[CH:3]=[C:4]([C:12]([CH3:15])([CH3:14])[CH3:13])[C:5]([OH:11])=[C:6]([C:8](=[N:21][OH:22])[CH3:9])[CH:7]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 1-(5-bromo-3-(tert-butyl)-2-hydroxyphenyl)ethanone (0.5 g, 1.8 mmol), NaOAc (246 mg, 3.0 mmol) and NH2OH.HCl (187 mg, 2.7 mmol) in EtOH (10 mL) was heated at reflux for 3 h, concentrated and the obtained solid was washed with water to give compound P8a (0.5 g, 97%) as solid.
Workup
- temperaturewas heated
- temperatureat reflux for 3 h
- concentrationconcentrated
- washthe obtained solid was washed with water
- customto give compound P8a (0.5 g, 97%) as solid
Sources & evidence
- ORD record
- ord-9cfe3a9d89924c158d21700b49d2719e
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08946446B2
Reaction notes
Loading…