Hydroxylamine → HCID 178513301, compound
Reaction equation
[F:1][C:2]([F:12])([F:11])[C:3]1[CH:10]=[CH:9][C:6]([C:7]#[N:8])=[CH:5][CH:4]=1.[NH2:13][OH:14]>C(O)C>[OH:14][NH:13][C:7](=[NH:8])[C:6]1[CH:9]=[CH:10][C:3]([C:2]([F:1])([F:11])[F:12])=[CH:4][CH:5]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 80 °C
Procedure
To a solution of 4-(trifluoromethyl)benzonitrile (10 g) in ethanol (100 ml) was added 50% hydroxylamine aqueous solution (11.6 g), and stirred at 80° C. overnight. After completion of the reaction, the solvent was evaporated, and water was added thereto. The insoluble matter was collected by filtration, and then dried to give N-hydroxy-4-(trifluoromethyl)benzamidine (12.6 g).
Workup
- customAfter completion of the reaction
- customthe solvent was evaporated
- additionwater was added
- filtrationThe insoluble matter was collected by filtration
- customdried
Sources & evidence
- ORD record
- ord-aeac104068884afc89d4dc3e5260a5f4
- Source dataset
- uspto-grants-2015_10
- Patent number
- US09150555B2
Reaction notes
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