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Potassium Nitrate → HCID 10588717, compound

HRID 1251007
Notes
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Reaction equation

HRID 1251007 reaction equation
[CH3:1][C:2]1[CH:11]=[CH:10][C:9]2[NH:8][C:7](=[O:12])[C:6](=[O:13])[NH:5][C:4]=2[C:3]=1[C:14]([O:16][CH3:17])=[O:15].[N+:18]([O-])([O-:20])=[O:19].[K+]>OS(O)(=O)=O>[CH3:17][O:16][C:14]([C:3]1[C:4]2[NH:5][C:6](=[O:13])[C:7](=[O:12])[NH:8][C:9]=2[CH:10]=[C:11]([N+:18]([O-:20])=[O:19])[C:2]=1[CH3:1])=[O:15]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 24434Potassium NitrateHCID 108472796-Methyl-2,3-dioxo-1,2,3,4-tetrahydro-quinoxaline-5-carboxylic Acid, Methyl Ester

Product 1

HCID 10588717HCID 10588717, compound

Reagents, catalysts & solvents 1

HCID 1118Sulfuric AcidSolvent

Procedure

To a solution of 6-methyl-2,3-dioxo-1,2,3,4-tetrahydro-quinoxaline-5-carboxylic acid, methyl ester (1.11 g, 4.74 mmol) in conc. H2SO4 (15 mL) at room temperature was added in one portion with vigorous stirring potassium nitrate (0.529 g, 5.23 mmol). The reaction mixture was stirred for 23 hours and poured over ice. The precipitated product was thoroughly washed with water upon collection to give 1.28 g (97%).

Workup

  1. additionpoured over ice
  2. washThe precipitated product was thoroughly washed with water upon collection
  3. customto give 1.28 g (97%)

Sources & evidence

ORD record
ord-b6baeb97acef4a659a296f3eeba14199
Source dataset
uspto-grants-2002_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06340758B1

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes