HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378451Generated: October 29, 2026
Potassium Hydroxide → HCID 15453202, compound
https://huagongshe.com/reaction/378451
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 15453201 | HCID 15453201 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15453202 | HCID 15453202 | 101.2% |
Reaction Steps
N-Benzenesulfonyl-N-(3-methyl-4-phenyl-5-isoxazolyl)benzenesulfonamide (300 mg, 0.66 mmol) was dissolved in methanol. Potassium hydroxide (300 mg, 5.5 mmol) was added and the solution was warmed to 45° C. to dissolve the sodium hydroxide. Stirring was continued for 20 min. Methanol was removed under reduced pressure. The residue was dissolved in water, cooled to 0° C. and acidified to pH 3-4 with concentrated HCl. The solid precipitate was extracted with ethyl acetate, dried and evaporated in vacuo to give 210 mg (100% yield) of N-(3-methyl-4-phenyl-5-isoxazolyl)benzenesulfonamide, which was further purified by recrystallization from ethyl acetate/hexanes, m.p. 124-126° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06030991 |
|---|
| Source dataset | uspto-grants-2000_02 |
|---|
| ORD ID | ord-e4bf02eab21946eca988f936fa770bf7 |
|---|
| Source note | uspto-grants-2000_02 |
|---|