HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Toluenesulfonyl chloride → 5-(4-(p-Toluenesulfonylamino)phenyl)thiazolidine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 5-(4-Aminophenyl)thiazolidine-2,4-dione | HCID 12850972 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 5-(4-(p-Toluenesulfonylamino)phenyl)thiazolidine-2,4-dione | HCID 19006060 | 74.7% |
Reaction Steps
Into 10 ml of pyridine were dissolved 0.50 g of 5-(4-amino-phenyl) thiazolidine-2,4-dione, and after added 0.46 g of p-toluenesulfonyl chloride, the mixture was stirred for 1 hour at room temperature. After the completion of reaction, the reaction mixture was poured into ice water, which was extracted with ethyl acetate. The organic layer was washed with 10% hydrochloric acid, washed with water and dried. Then, solvent was distilled off. The residue was recrystallized from benzene to obtain 0.65 g of title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05342850 |
| Source dataset | uspto-grants-1994_08 |
| ORD ID | ord-a9d060056e9d435e97a88f6f23bac97d |
| Source note | uspto-grants-1994_08 |