Nitric Acid → HCID 70379606, compound
Reaction equation
[F:1][CH:2]([O:7][C:8]1[CH:13]=[CH:12][C:11]([N:14]2[CH2:18][CH2:17][O:16][C:15]2=[O:19])=[CH:10][CH:9]=1)[C:3]([F:6])([F:5])[F:4].[N+:20]([O-])([OH:22])=[O:21]>S(=O)(=O)(O)O>[N+:20]([C:12]1[CH:13]=[C:8]([O:7][CH:2]([F:1])[C:3]([F:5])([F:4])[F:6])[CH:9]=[CH:10][C:11]=1[N:14]1[CH2:18][CH2:17][O:16][C:15]1=[O:19])([O-:22])=[O:21]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2.79 g (10 mmoles) of the oxazolidinon of Step 2 are dissolved in 7 ml concentrated sulfuric acid and nitrated at 0° C. with a mixture of 0.43 ml (10 mmoles) fuming nitric acid and 3.6 ml concentrated sulfuric acid.
Sources & evidence
- ORD record
- ord-72f79cdae65c44ccb44f9b771dbd7ecc
- Source dataset
- uspto-grants-1989_07
- Patent number
- US04845294
Reaction notes
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