HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852435Generated: November 1, 2026
Sodium Hydroxide → 5-Bromo-3-hydroxy-2,3-dihydrobenzothiophene 1,1-Dioxide
https://huagongshe.com/reaction/1852435
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzo[b]thiophene, 5-bromo-, 1,1-dioxide | HCID 23261743 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | 5-Bromo-3-hydroxy-2,3-dihydrobenzothiophene 1,1-Dioxide | HCID 86729352 | — |
Reaction Steps
5-Bromo-1-benzothiophene 1,1-dioxide (100 mg, 0.41 mmol) was suspended in 1N aqueous sodium hydroxide (2.0 mL), heated to 100° C. in a microwave, and allowed to stir for 15 minutes. The mixture was then allowed to cool to ambient temperature before the mixture was diluted with saturated aqueous ammonium chloride and extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous MgSO4, filtered, and concentrated in vacuo. The residue was used without further purification. LRMS (ESI) calc'd for C8H7BrO3S [M+Na]+: 285. Found: 285.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962608B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-a709b100a83144a59508c20da3a20b0a |
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| Source note | uspto-grants-2015_02 |
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