Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 69037483 | HCID 69037483 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69036733 | HCID 69036733 | — |
Reaction Steps
To 3.3 mmol 2-isobutoxy-5-methylsulfamoyl-benzoic acid methyl ester in 10 ml THF was added 20 mmol 2 M aq NaOH, and the mixture was heated at 50° C. for 2 h. The mixture was then cooled to RT and extracted twice with ether. The aqueous phase was acidified with 10% aq citric acid and extracted 3 times with ethyl acetate. The combined organic phases were dried with Na2SO4. Evaporation in vacuo followed by trituration in ether afforded the title compound. MS (m/e): 286.2 ([M−H]−, 100%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07605163B2 |
|---|
| Source dataset | uspto-grants-2009_10 |
|---|
| ORD ID | ord-ac60dc8835a84f7bbd216969f552467c |
|---|
| Source note | uspto-grants-2009_10 |
|---|