HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminophenol → N-(2-hydroxyphenyl)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminophenol | HCID 5801 | — |
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-(2-hydroxyphenyl)benzenesulfonamide | HCID 231991 | 44.2% |
Reaction Steps
A flask with a stirrer was charged with 10.9 g of 2-aminophenol, 10.1 g of triethylamine and 100 ml of acetone, and a solution of 17.7 g of benzenesulfonyl chloride in 50 ml of acetone was dropwise added with cooling with ice over 30 minutes. After completion of the addition, the reaction mixture was stirred at room temperature for 2 hours and then poured into 500 ml of ice water. A precipitated crystal was recovered by filtration and washed with water. The obtained crystal was recrystallized from ethyl acetate/n-hexane mixed solvents, to give 11.0 g of an end product. Melting point 140.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06921740B1 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-48c95e3620254e9a963d4eab7f027d0f |
| Source note | uspto-grants-2005_07 |