Hydroxyamine hydrochloride → HCID 72346776, compound
Reaction equation
[CH3:1][S:2][C:3]1[O:7][C:6]([CH:8]=O)=[CH:5][CH:4]=1.Cl.[NH2:11][OH:12].C([O-])(=O)C.[Na+]>C(O)C>[CH3:1][S:2][C:3]1[O:7][C:6]([CH:8]=[N:11][OH:12])=[CH:5][CH:4]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 23 °C
Procedure
To a solution of 5-(methylthio)furan-2-carbaldehyde (1.0 g, 7.04 mmol) in ethanol (10 mL) was added an aqueous solution of hydroxylamine hydrochloride (3.75M) (2.26 mL, 8.45 mmol) and an aqueous solution of sodium acetate (1.5 M) (3.78 mL, 5.63 mmol). The reaction mixture was stirred a 23° C. for 18 hours. The ethanol was concentrated in vacuo, H2O was added (50 mL) and the precipitate was filtered and dried in oven (60° C.) for 10 minutes to afford 277 mg (25%) of the title compound. LCMS (+ESI, M+H+) m/z 158.
Workup
- concentrationThe ethanol was concentrated in vacuo, H2O
- additionwas added (50 mL)
- filtrationthe precipitate was filtered
- customdried in oven (60° C.) for 10 minutes
Sources & evidence
- ORD record
- ord-8b8574e7a6094b56bb9615673cf4abdc
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07893055B2
Reaction notes
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