Sulfuric Acid → 4-Trifluoromethyl-2-nitrobenzenediazonium Bisulfate
Reaction equation
[S:1](=[O:5])(=[O:4])([OH:3])[OH:2].[NH2:6][C:7]1[CH:12]=[CH:11][C:10]([C:13]([F:16])([F:15])[F:14])=[CH:9][C:8]=1[N+:17]([O-:19])=[O:18].[N:20]([O-])=O.[Na+]>O>[S:1](=[O:3])(=[O:2])([OH:5])[O-:4].[F:14][C:13]([F:16])([F:15])[C:10]1[CH:11]=[CH:12][C:7]([N+:6]#[N:20])=[C:8]([N+:17]([O-:19])=[O:18])[CH:9]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 75 °C
Procedure
To a 500 mL three-necked flask equipped with a mechanical stirrer is added 99.5 g of concentrated sulfuric acid and 62.5 g of 4-trifluoro-2-nitroaniline (or 4-amino-3-nitro-benzotrifluoride). After heating to 75° C., 200 g of water is added at which time the temperature is reduced to 0° C. Sodium nitrite solution (52.9 g, 40% by weight in water) is added over two hours while maintaining the temperature at 0-5° C. The title diazonium salt solution (351 g) is filtered and stored at −15° C. for later use.
Workup
- customTo a 500 mL three-necked flask equipped with a mechanical stirrer
- customis reduced to 0° C
- temperaturewhile maintaining the temperature at 0-5° C
- filtrationThe title diazonium salt solution (351 g) is filtered
- customstored at −15° C. for later use
Sources & evidence
- ORD record
- ord-c9439d5c254548ed979ee5f8388faadd
- Source dataset
- uspto-grants-2002_05
- Patent number
- US06392056B1
Reaction notes
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