Potassium Nitrate → HCID 22097096, compound

HRID 1458840Notes

Reaction equation

[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]([CH:12]1[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]1)[C:7](=[O:18])[C:6](=[O:19])[NH:5]2.[N+:20]([O-])([O-:22])=[O:21].[K+]>S(=O)(=O)(O)O>[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[N+:20]([O-:22])=[O:21])[N:8]([CH:12]1[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]1)[C:7](=[O:18])[C:6](=[O:19])[NH:5]2

Participants

Conditions

Temperature: 25 °C

Procedure

26.3 g (94 mmol) of 6-Chloro-1-cyclohexyl-2,3(1H,4H)-quinoxalinedione were dissolved in 275 ml of concentrated sulfuric acid and then, at 0° C., 9.5 g (94 mmol) of potassium nitrate were added a little at a time. The mixture was then stirred at 0° C. for 30 min and at 25° C. for 2 h and poured into ice-water. The precipitate was filtered off with suction to yield 29.5 g (97%) of the product.

Workup

filtrationThe precipitate was filtered off with suction

Sources & evidence

ORD record: ord-1d8ade5707cb4aa59984edcf5ecaad94
Source dataset: uspto-grants-1998_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05852017

Reaction notes

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