HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 3-{[(3-Fluorophenyl)amino]sulfonyl}benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 3-{[(3-fluorophenyl)amino]sulfonyl}benzoate | HCID 66676257 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-{[(3-Fluorophenyl)amino]sulfonyl}benzoic acid | HCID 766536 | — |
Reaction Steps
To the product of Step A was added ethanol (6.4 mL) followed by a solution of NaOH (0.483 g, 12.1 mmol) in water (6.4 mL). The reaction was stirred at ambient temperature for 1 hour. To the mixture was added 1 NHCl (22.8 mL), and the mixture stirred at ambient temperature overnight. The solids were collected by filtration, washed with water (2×4 mL) and dried in a vacuum oven at 45° C. overnights to give 3-{[(3-fluorophenyl)amino]sulfonyl}benzoic acid: 1H NMR (400 MHz, DMSO-d6) δ ppm 13.51 (bs, 1H), 10.68 (bs, 1H), 8.30 (t, J=1.8, 1H), 8.14 (dt, J=7.7, 1.4, 1H), 7.99 (ddd, J=7.8, 2.0, 1.1, 1H), 7.70 (t, J=7.8, 1H), 7.27 (m, 1H), 6.94-6.82 (m, 3H); MS (ESI) m/z 294 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08404719B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-69274046df0848aa9d79d783c2a64056 |
| Source note | uspto-grants-2013_03 |