HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophene-3-carboxylic acid → 5-Bromothiophene-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophene-3-carboxylic acid | HCID 6918 | — |
| Reactant | Bromine | HCID 24408 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-Bromothiophene-3-carboxylic acid | HCID 12039978 | 80% |
Reaction Steps
Under a nitrogen atmosphere, 3-thiophenecarboxylic acid (10 g, 78 mmol) was added to acetic acid (100 ml), and bromine (12.5 g, 78 mmol) was then slowly dropped and stirred at the same temperature for one hour. Then, ice (300 g) was added. By filtering a precipitated white solid and then drying the white solid after washing with water, a target substance was obtained as a white solid (80% yield). 1H-NMR (400 MHZ, CDCl3, TMS) δ 8.12 (s, 1 H), 7.51 (s, 1 H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09312491B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-c2580f4780f44bd095275368034c4f89 |
| Source note | uspto-grants-2016_04 |