HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium hydroxide, monohydrate → (3-Ethylsulfamoyl-phenyl)-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | (3-Ethylsulfamoyl-phenyl)-acetic acid methyl ester | HCID 57421970 | — |
| Solvent | Citric Acid | HCID 311 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (3-Ethylsulfamoyl-phenyl)-acetic acid | HCID 57421971 | 99% |
Reaction Steps
(3-Ethylsulfamoyl-phenyl)-acetic acid methyl ester (0.28 g, 1.1 mmol) was dissolved in THF and LiOH hydrate (63 mg, 1.5 mmol) in water was added. The reaction mixture was stirred at room temperature for 4 hours and then diluted with ethyl acetate and 10% citric acid. The organic layer was washed with brine, dried over sodium sulfate, and concentrated to a solid. 0.25 g, 1.1 mmol 99% yield. 1H NMR 500 MHz (DMSO) 7.71 ppm, 1H, s; 7.70 ppm, 1H, m; 7.50 ppm, 3H, m; 4.11 ppm, 1H, br s; 3.70 ppm, 2H, s; 2.81 ppm, 2H, m; 0.99 ppm, 3H, t.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07514448B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-94ac38098308457683554da4a2bcb3a8 |
| Source note | uspto-grants-2009_04 |