HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-Chlorobenzo[b]thien-2-yl)ethanone → HCID 22473621, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-Chlorobenzo[b]thien-2-yl)ethanone | HCID 12398628 | — |
| Reactant | Phenyltrimethylammonium bromide dibromide | HCID 17977687 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22473621 | HCID 22473621 | 124% |
Reaction Steps
A mixture of 1-(4-chlorobenzo[b]thiophen-2-yl]ethan-1-one (1.67 g), phenyltrimethylammonium tribromide (2.98 g) and tetrahydrofuran (40 ml) was stirred under nitrogen at ambient temperature for 22.5 hours then it was filtered and diluted with water (150 ml). The product was extracted into dichloromethane (3×30 ml), the combined extracts were dried (MgSO4) and the solvents were removed in vacuo. The residue was purified by flash chromatography over silica using dichloromethane as eluant. Appropriate fractions were combined and the solvents removed in vacuo to leave 2-bromo-1-(4-chlorobenzo[b]thiophen-2-yl]ethan-1-one (1.65 g) as an off-white solid, m.p. 116-118° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06900216B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-3fcd3f1f0c7443b7baba08706dd00a10 |
| Source note | uspto-grants-2005_05 |