HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Sodium 2-amino-3-(2-thienyl)benzenesulphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium 2-amino-5-bromo-3-(2-thienyl)benzenesulphonate | HCID 23687032 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Sodium 2-amino-3-(2-thienyl)benzenesulphonate | HCID 23687031 | — |
Reaction Steps
21 g (59 mmol) of sodium 2-amino-5-bromo-3-(2-thienyl)benzenesulphonate are heated at 100° C. for 1 hour in the presence of 350 ml of 10% sodium hydroxide solution, 15 ml of ethanol and 7.4 g of zinc. The temperature of the reaction medium is allowed to return to room temperature and 300 ml of methanol are added. The mixture is filtered through Celite, the filtrate is concentrated and the residue is taken up in 1N sodium hydroxide solution at 0° C. and dried under vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05739382 |
| Source dataset | uspto-grants-1998_04 |
| ORD ID | ord-14cc9611c01f4388bf776ca50731be0e |
| Source note | uspto-grants-1998_04 |