Potassium Nitrate → HCID 23296614, compound
Reaction equation
[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[C:3]1[CH2:11][CH2:12][C:13]1[CH:20]=[CH:19][C:16]([C:17]#[N:18])=[CH:15][CH:14]=1.[N+:21]([O-])([O-:23])=[O:22].[K+]>S(=O)(=O)(O)O>[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][C:7]([N+:21]([O-:23])=[O:22])=[CH:8][CH:9]=2)[CH:4]=[C:3]1[CH2:11][CH2:12][C:13]1[CH:14]=[CH:15][C:16]([C:17]#[N:18])=[CH:19][CH:20]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 2 °C
Procedure
Within 2 hours 1.7 g (6.53 mmol) of 4-[2-(1-methyl-indol-2-yl)ethyl]benzonitrile is dissolved in 20 ml conc. sulphuric acid at 15° C. and then cooled to 2° C. Then 0.66 g (6.53 mmol) of potassium nitrate are added batchwise (temperature rise to about 10° C.). The mixture is stirred for a further 30 minutes at 2-5° C. and then poured onto ice. The yellowish precipitate formed is filtered off and washed with water.
Workup
- additionpoured onto ice
- customThe yellowish precipitate formed
- filtrationis filtered off
- washwashed with water
Sources & evidence
- ORD record
- ord-8cbb750bedee41b59ed9df6abada1f36
- Source dataset
- uspto-grants-2000_09
- Patent number
- US06121308
Reaction notes
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