HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Acetylthiophene → 2-Bromo-1-(thiophen-2-yl)ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Acetylthiophene | HCID 6920 | — |
| Reactant | Bromine | HCID 24408 | — |
| Catalyst | Acetic Acid Mixture with Hydrobromic Acid | HCID 21893785 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Bromo-1-(thiophen-2-yl)ethan-1-one | HCID 2776372 | 37% |
Reaction Steps
To a solution of 500 mg (3.96 mmol) of 2-acetyl thiophene (Aldrich Chemical Co.) dissolved in 20 mL of CHCl3, was added 1 drop of 30% HBr/CH3COOH (Aldrich Chemical Co.) followed by 3.96 mmol (633 mg; 204 μL) of bromine (Aldrich Chemical Co.) added dropwise over 30 min. The reaction was allowed to stir for 1 h. The solution was concentrated to an oil and dried in vacuo. The crude product was purified on 1 mm silica prep plates eluting with neat CH2Cl2 to obtain 300 mg (37% yield) of 2-bromo-1-(2-thienyl)ethan-1-one. 1H-NMR (CDCl3; 300 MHz) δ 7.8 (m, 2H), 7.18 (m, 1H), 4.37 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06492403B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-c4dec4485dcc482c86f7fd771b3fd833 |
| Source note | uspto-grants-2002_12 |