Benzenamine, 3,4-dichloro-N-hydroxy- → HCID 21553680, compound
Reaction equation
[Cl:1][C:2]([N:5]=[C:6]=[O:7])([Cl:4])[Cl:3].[Cl:8][C:9]1[CH:10]=[C:11]([NH:16][OH:17])[CH:12]=[CH:13][C:14]=1[Cl:15]>C(OCC)C>[Cl:1][C:2]([Cl:4])([Cl:3])[NH:5][C:6]([N:16]([C:11]1[CH:12]=[CH:13][C:14]([Cl:15])=[C:9]([Cl:8])[CH:10]=1)[OH:17])=[O:7]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of trichloromethyl isocyanate (16 grams; 0.1 mol) in diethyl ether (40 ml) is added dropwise, with stirring, to a solution of N-(3,4-dichlorophenyl) hydroxylamine (17.8 grams; 0.1 mol) in diethyl ether (60 ml) at room temperature. Stirring is continued for a period of about 1 hour resulting in the formation of a precipitate. The precipitate is recovered by filtration, is washed and dried to yield 1-trichloromethyl-3-(3',4'-dichlorophenyl)-3-hydroxyurea.
Workup
- customresulting in the formation of a precipitate
- filtrationThe precipitate is recovered by filtration
- washis washed
- customdried
Sources & evidence
- ORD record
- ord-d9d79acedcee4e29b26e339a70b388de
- Source dataset
- uspto-grants-1976_03
- Patent number
- US03944410
Reaction notes
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