HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → 5-(4-Benzoylaminophenyl)thiazolidine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 5-(4-Aminophenyl)thiazolidine-2,4-dione | HCID 12850972 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 5-(4-Benzoylaminophenyl)thiazolidine-2,4-dione | HCID 19006059 | 93.3% |
Reaction Steps
Into 20 ml of dioxane were dissolved 0.5 g of 5-(4-aminophenyl) thiazolidine-2,4-dione, and, after added 0.34 g of benzoyl chloride and further added dropwise 0.24 g of triethylamine, the mixture was refluxed for 1 hour. After cooling by standing, the reaction mixture was poured into 150 ml of ice water and the crystals deposited were collected by filtration, washed with water and dried. These were recrystallized from chloroform to obtain 0.70 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-9beb242176cd4c92aac25d7e1e4edc8e |
| Source note | uspto-grants-1994_08 |