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Potassium Nitrate → HCID 10588717, compound

HRID 1282295
Notes
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Reaction equation

HRID 1282295 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-d6d81e580c7c4367b3edd88b66f64788
Source dataset
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06455698B1

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes