Hydroxylamine → 16348-49-5
Reaction equation
[C:1](#[N:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[NH2:4].[NH2:10][OH:11]>CCO>[NH2:4][C:3]1[CH:5]=[CH:6][CH:7]=[CH:8][C:2]=1[C:1](=[N:10][OH:11])[NH2:9]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Anthranilonitrile (1 g, 8,5 mmol) and hydroxylamine (50% in water, 0.57 cm3, 9.3 mmol, 1.1 eq) in EtOH (42.5 cm3) were stirred under reflux for 24 hours, after which the volatiles were removed under reduced pressure and residue was partitioned between water (5 cm3) and CH2Cl2 (100 cm3). The organic phase was evaporated to dryness in the rotary evaporator followed by high vacuum line to give the product 2-amino-N′-hydroxybenzimidamide (1.16 g, 90.3%) as a solid, mp 85-86° C.
Workup
- temperatureunder reflux for 24 hours
- customafter which the volatiles were removed under reduced pressure and residue
- customwas partitioned between water (5 cm3) and CH2Cl2 (100 cm3)
- customThe organic phase was evaporated to dryness in the rotary evaporator
Sources & evidence
- ORD record
- ord-8f1f5d3da15840fba581673c7ed7ff59
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07838483B2
Reaction notes
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