Hydrochloric Acid → HCID 21541623, compound

HRID 1076057Notes

Reaction equation

HRID 1076057 reaction equation
[C:1]1([C:20]([O-:22])=[O:21])[C:10]2[CH:9]=[C:8]([C:11]([O-:13])=[O:12])[CH:7]=[C:6]([C:14]([O-:16])=[O:15])[C:5]=2[CH:4]=[C:3]([C:17]([O-:19])=[O:18])[CH:2]=1.[K+].[K+].[K+].[K+].Cl>O>[C:1]1([C:20]([OH:22])=[O:21])[C:10]2[CH:9]=[C:8]([C:11]([OH:13])=[O:12])[CH:7]=[C:6]([C:14]([OH:16])=[O:15])[C:5]=2[CH:4]=[C:3]([C:17]([OH:19])=[O:18])[CH:2]=1

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 21541626HCID 21541626, compound

Product 1

HCID 21541623HCID 21541623, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

Crude tetrapotassium 1,3,5,7-naphthalenetetracarboxylate obtained in Example 13 was again dissolved in water, and the solution was acidified with hydrochloric acid to an acidity lower than pH 1 to form free crude 1,3,5,7-naphthalenetetracarboxylic acid. The product was separated and dried to form crude 1,3,5,7-naphthalenetetracarboxylic acid as shown in Table 7.

Workup

  1. customto form free crude 1,3,5,7-naphthalenetetracarboxylic acid
  2. customThe product was separated
  3. customdried

Sources & evidence

ORD record
ord-4f61670b33994023acccadebe898a47f
Source dataset
uspto-grants-1976_05
Patent number
US03954840

Reaction notes

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