HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromo-4-methylthiophene-2-sulfonamide → 4-Methylthiophene-2-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromo-4-methylthiophene-2-sulfonamide | HCID 22019533 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-Methylthiophene-2-sulfonamide | HCID 600929 | 43% |
Reaction Steps
To a stirred solution of 5-bromo-4-methylthiophene-2-sulfonamide (3.1 g, 12.1 mmol) in AcOH (30 mL) is added zinc dust (2.4 g, 36.2 mmol). The reaction mixture is heated to reflux for 8 hr. After 8 hr, the reaction mixture is cooled and filtered. The filtrate is neutralized with 1 M NaOH. The aqueous layer is extracted with EtOAc (300 mL). The organics are dried (Na2SO4), filtered and concentrated in vacuo. The crude product is chromatographed on silica gel, eluting with CH2Cl2 to afford the title compound (0.90 g, 43%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07084170B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-d567173a966040fe8fce61a1b01b4a96 |
| Source note | uspto-grants-2006_08 |