HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → Ethyl 2-chloro-5-sulfamoylthiophene-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 2-Chloro-5-sulfamoylthiophene-3-carboxylic acid | HCID 1201498 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-chloro-5-sulfamoylthiophene-3-carboxylate | HCID 19106450 | — |
Reaction Steps
To a round bottom flask were added 5-chloro-4-carboxythiophene-2-sulfonamide (5.0 g, 20.7 mmole) along with toluene (25 mL), ethanol (20 ml), and conc. H2SO4 (25 drops). The reaction mixture was refluxed for 96 hours. The reaction mixture was cooled and the solvent was removed under vacuum. The residue was then poured onto ice and the pH adjusted to ~8.0 using 10% sodium carbonate. The basic aqueous layer was extracted with ethyl acetate and the organic layer was washed with water, brine, and dried (MgSO4). Solvent removal yielded 3.92 g (70%) of an off white solid which was used as is: mp =98°-99° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05276025 |
| Source dataset | uspto-grants-1994_01 |
| ORD ID | ord-8077273d383c4c3991829319258dbb7d |
| Source note | uspto-grants-1994_01 |