HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methylthiophene → 5-Methylthiophene-2-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methylthiophene | HCID 11126 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Product | 5-Methylthiophene-2-sulfonamide | HCID 600930 | — |
Reaction Steps
The procedure of Example 3 was followed using 2-methylthiophene (8.0 g, 81.6 mmole), chlorosulfonic acid (28.4 g, 245 mmole) and 200 ml concentrated ammonium hydroxide to produce 5-methyl-2-thiophenesulfonamide which was contacted with 3,4-dichlorophenyl isocyanate (2.61 g, 13.8 mmole) and 1N NaOH (14.5 ml) in 10 ml acetone to provide 3.5 g of the named product as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05302724 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-67a63ffbed1c4417a75e9f01866150d9 |
| Source note | uspto-grants-1994_04 |