Phthalic Anhydride → Phthalimidomethanesulfonic acid potassium salt

HRID 1390708Notes

Reaction equation

HRID 1390708 reaction equation
[NH2:1][CH2:2][S:3]([OH:6])(=[O:5])=[O:4].C([O-])(=O)C.[K+:11].[C:12]1(=O)[O:17][C:15](=[O:16])[C:14]2=[CH:18][CH:19]=[CH:20][CH:21]=[C:13]12>C(O)(=O)C>[K+:11].[C:12]1(=[O:17])[N:1]([CH2:2][S:3]([O-:6])(=[O:5])=[O:4])[C:15](=[O:16])[C:14]2=[CH:18][CH:19]=[CH:20][CH:21]=[C:13]12

Participants

5

Reactant 3

HCID 6811Phthalic AnhydrideHCID 83791Aminomethanesulfonic acidHCID 517044Potassium Acetate

Product 1

HCID 88789710Phthalimidomethanesulfonic acid potassium salt

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Procedure

A suspension of 15.1 g. (0.136 mol.) of aminomethanesulfonic acid and 14.2 g. (0.145 mol.) of anhydrous potassium acetate in 48 ml. of acetic acid is refluxed for ten minutes. Phthalic anhydride (21.4 g., 0.145 mol.) is then added and the resulting mixture is refluxed for 2.5 hours. The product is collected by filtration and washed with acetic acid and ethanol to give phthalimidomethanesulfonic acid potassium salt.

Workup

  1. additionA suspension of 15.1 g
  2. temperaturethe resulting mixture is refluxed for 2.5 hours
  3. filtrationThe product is collected by filtration
  4. washwashed with acetic acid and ethanol

Sources & evidence

ORD record
ord-894285b2dc1f41598bb5d4e064c3a9d9
Source dataset
uspto-grants-1979_02
Patent number
US04139701

Reaction notes

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