Sodium Methoxide → HCID 70392361, compound

HRID 1381661Notes

Reaction equation

HRID 1381661 reaction equation
C[O-].[Na+:3].[CH:4]1[C:17]2[NH:16][C:15]3[CH:14]=[CH:13][CH:12]=[C:11]([C:18]([OH:20])=[O:19])[C:10]=3[O:9][C:8]=2[C:7]([C:21]([OH:23])=[O:22])=[CH:6][CH:5]=1>CO>[Na+:3].[CH:4]1[C:17]2[NH:16][C:15]3[CH:14]=[CH:13][CH:12]=[C:11]([C:18]([O-:20])=[O:19])[C:10]=3[O:9][C:8]=2[C:7]([C:21]([O-:23])=[O:22])=[CH:6][CH:5]=1.[Na+:3]

Participants

4

Reactant 2

HCID 10942334Sodium MethoxideHCID 14031272HCID 14031272, compound

Product 1

HCID 70392361HCID 70392361, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

Sodium methoxide (82 mg) is added to a solution of phenoxazine 4,6-dicarboxylic acid in methanol (5 ml). The solution is then evaporated to dryness to afford phenoxazine 4,6-dicarboxylic acid sodium salt. This compound may be converted to salts such as potassium, lithium, ammonium, calcium, magnesium, ferrous, zinc, copper, manganous, aluminum, ferric, manganic salts and the like using similar methods.

Workup

  1. customThe solution is then evaporated to dryness

Sources & evidence

ORD record
ord-9d4ca859b47b48fca8ff4ea69d33c107
Source dataset
uspto-grants-1989_02
Patent number
US04803269

Reaction notes

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