Hydrochloric Acid → HCID 23207676, compound
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.[N:14]([O-])=O.[Na+].[ClH:18]>[Cl-].[Zn+2].[Cl-]>[Cl-:18].[C:3]1([C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)[C:2]([N+:1]#[N:14])=[CH:7][CH:6]=[CH:5][CH:4]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
First, 500 mg of o-aminobiphenyl was dissolved in 2.4 ml of 13.6% hydrochloric acid (4 molar equivalents), and the resulting solution was subjected to ultrasonic treatment for 10 minutes and then kept at the freezing point. To the solution at the freezing point was added dropwise 0.8 ml of a 25 % aqueous solution of sodium nitrite (1 molar equivalent) slowly while stirring. After the addition, the mixture was stirred at the freezing point for 2 hours, followed by addition of 0. 6 ml of saturated zinc chloride while stirring at the freezing point. This caused precipitation of zinc chloride double salt of diazonium chloride.
Workup
- additionAfter the addition
- stirringthe mixture was stirred at the freezing point for 2 hours
- additionfollowed by addition of 0
- customThis caused precipitation of zinc chloride double salt of diazonium chloride
Sources & evidence
- ORD record
- ord-109446e4d0244396b646e2bdb8984b7c
- Source dataset
- uspto-grants-1996_01
- Patent number
- US05480791
Reaction notes
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