Potassium Nitrate → HCID 178481719, compound
Reaction equation
[N+:1]([O-:4])([O-])=[O:2].[K+].[OH:6][C:7]1[C:16]([OH:17])=[N:15][C:14]2[C:13]3=[N:18][N:19]([CH3:21])[N:20]=[C:12]3[CH:11]=[CH:10][C:9]=2[N:8]=1>>[OH:6][C:7]1[C:16]([OH:17])=[N:15][C:14]2[C:13]3=[N:18][N:19]([CH3:21])[N:20]=[C:12]3[C:11]([N+:1]([O-:4])=[O:2])=[CH:10][C:9]=2[N:8]=1Participants
3
Conditions
- Temperature
- 0 °C
Procedure
Finely powdered potassium nitrate (0.47 g, 4.6 mmol) was added to an ice-cooled solution of 7,8-dihydroxy-2-methyl-2H-1,2,3-triazolo[4,5-f]quinoxaline (1.0 g, 4.6 mmol). The mixture was stirred at 0° C. for 11/2 h, then at room temperature for 4 h and finally poured into ice/water. The resulting solution was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate and concentrated to dryness giving 0.27 g (22%) of the nitro compound; m.p.>300° C.; IR (KBr): 1700 cm-1 ; 1H-NMR (DMSO-d6): 4.63 (s, 3H, CH3), 8.15 (s, 1H, ArH), 12.1 (broad s, 1H, OH), 13.0 (broad s, 1H, OH).
Workup
- waitat room temperature for 4 h
- extractionThe resulting solution was extracted with ethyl acetate
- dry with materialThe extract was dried over anhydrous sodium sulfate
- concentrationconcentrated to dryness
Sources & evidence
- ORD record
- ord-322addac198c43e5a5fae472879d94ae
- Source dataset
- uspto-grants-1991_10
- Patent number
- US05057516
Reaction notes
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