HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → 5-Amidino-2-benzoyloxybenzenesulfonic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | 5-Amidino-2-hydroxybenzenesulfonic acid | HCID 135598748 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 5-Amidino-2-benzoyloxybenzenesulfonic acid | HCID 13178455 | — |
Reaction Steps
To 30 ml of dried pyridine, was added 3.0 g of 5-amidino-2-hydroxybenzenesulfonic acid. To the mixture, while being cooled in ice, was slowly added dropwise 2.0 g of benzoyl chloride. After the addition, the mixture was stirred overnight at room temperature. The insolubles deposited from the reaction mixture were separated by filtration, washed with pyridine, then with water, finally with acetone, and suspended in methanol. The insolubles were removed by filtration, and ethyl ether was added to the filtrate to precipitate a colorless solid. The solid was collected by filtration and recrystallized from a methanol-ethyl ether mixture to obtain 5-amidino-2-benzoyloxybenzenesulfonic acid in colorless solid form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04514416 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-703e5952593c45aa8319c79932bf75bd |
| Source note | uspto-grants-1985_04 |