HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 5-Bromothiophene-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Thiophene-3-carboxylic acid | HCID 6918 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-Bromothiophene-3-carboxylic acid | HCID 12039978 | 61.8% |
Reaction Steps
To a solution of thiophene-3-carboxylic acid (12.6 g, 0.1 mol) in AcOH (96 ml), being stirred at room temperature, HBr solution (8 ml) was added, and the stirring continued until the color of mixture turned to yellow. Pyridinium bromide perbromide (27 g) was then sequentially added. The mixture was poured into ice-water, stirred for about 30 minutes. A white precipitate was formed, which was filtered and dried to obtain 5-bromo-thiophene-3-carboxylic acid (10.8 g) as a white solid after crystallization in hot water. HPLC: 92%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09249154B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-47026f3ddbd74f558f7d3ac670e56252 |
| Source note | uspto-grants-2016_02 |