HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Acetyl-N-(2-hydroxyethyl)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | 4-Acetylbenzenesulfonyl chloride | HCID 266418 | — |
| Reactant | Sodium 4-acetylbenzenesulphonate | HCID 23668814 | — |
| Product | 4-Acetyl-N-(2-hydroxyethyl)benzenesulfonamide | HCID 22750307 | — |
Reaction Steps
The damp 4-acetylbenzenesulfonyl chloride from 100 g. of sodium 4-acetylbenzenesulfonate is added to a stirred solution of 500 ml. of 50% aqueous 2-hydroxyethylamine. The mixture is stirred at room temperature for 16 hours, then acidified with hydrochloric acid and cooled to 0°-5° C. The precipitate of 4-acetyl-N-(2-hydroxyethyl)benzenesulfonamide is collected by filtration, washed with water and dried; m.p. 119°-121° C. after crystallization from water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04137408 |
| Source dataset | uspto-grants-1979_01 |
| ORD ID | ord-84f0f435abf9451bb67a39a34240a0aa |
| Source note | uspto-grants-1979_01 |