Nitric Acid → HCID 13135500, compound
Reaction equation
[N:1]1([CH:6]2[CH2:15][CH2:14][C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:7]2=[O:16])[CH:5]=[CH:4][N:3]=[CH:2]1.[N+:17]([O-:20])([OH:19])=[O:18]>>[N+:17]([O-:20])([OH:19])=[O:18].[N:1]1([CH:6]2[CH2:15][CH2:14][C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:7]2=[O:16])[CH:5]=[CH:4][N:3]=[CH:2]1Participants
3
Procedure
By proceeding analogously 2-(1-imidazolyl)-3,4-dihydro-1(2H)-naphthalenone was prepared, that, treated with a stoichiometric amount of nitric acid, gave 2-(1-imidazolyl)-3,4-dihydro-1(2H)-naphthalenone nitrate;
Workup
- customwas prepared
Sources & evidence
- ORD record
- ord-1e8c4600a4aa4025a71eea0a7644b596
- Source dataset
- uspto-grants-1986_05
- Patent number
- US04588738
Reaction notes
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