Sodium Methoxide → HCID 70392361, compound

HRID 247382Notes

Reaction equation

HRID 247382 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-6fa7b37d988a41e6aa6bbd02e095af4e
Source dataset
uspto-grants-1987_11
Patent number
US04707473

Reaction notes

Loading…