HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6959Generated: October 28, 2026
5-Bromo-4-chlorothiophene-2-sulfonamide → 4-Chlorothiophene-2-sulfonamide
https://huagongshe.com/reaction/6959
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Bromo-4-chlorothiophene-2-sulfonamide | HCID 2740062 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-Chlorothiophene-2-sulfonamide | HCID 22019465 | 52% |
Reaction Steps
To a stirred solution of 5-bromo-4-chlorothiophene-2-sulfonamide (2.4 g, 8.7 mmol) in AcOH (20 mL) is added zinc dust (1.7 g, 26.0 mmol). The reaction mixture is heated to 120° C. for 6 hr. After 6 hr, the mixture is filtered and neutralized with 1 M NaOH. The aqueous layer is extracted with EtOAc (2×100 mL). The combined organic extracts are dried (Na2SO4), filtered and concentrated in vacuo. The crude product is chromatographed on silica gel, eluting with CH2Cl2 to afford the title compound (0.88 g, 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07084170B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-ee96dca7353343b0ab451e1a1c0600f7 |
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| Source note | uspto-grants-2006_08 |
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