Nitric Acid → HCID 14988423, compound
Reaction equation
[C:1]1(=[O:14])[C:11]2=[C:12]3[C:7](=[CH:8][CH:9]=[CH:10]2)[CH2:6][CH2:5][CH2:4][N:3]3[C:2]1=[O:13].[N+:15]([O-])([OH:17])=[O:16]>>[N+:15]([C:9]1[CH:8]=[C:7]2[C:12]3=[C:11]([C:1](=[O:14])[C:2](=[O:13])[N:3]3[CH2:4][CH2:5][CH2:6]2)[CH:10]=1)([O-:17])=[O:16]Participants
3
Procedure
To a stirred fuming nitric acid (20 ml) at 0° C. was added 5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinoline-1,2-dione (5 g) portionwise. The reaction mixture was stirred for additional one hour, poured into ice water and the resultant precipitate was collected by filtration. This precipitate was washed with water and dried to yield the title compound. The compound was recrystallized from ethanol-hexane to give 3.8 g (61%) as yellow needles, mp 198°-199° C.
Workup
- filtrationthe resultant precipitate was collected by filtration
- washThis precipitate was washed with water
- customdried
Sources & evidence
- ORD record
- ord-f1fb21c237d44492b992c00aac405564
- Source dataset
- uspto-grants-1992_09
- Patent number
- US05147874
Reaction notes
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