HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Disulfide → 3-(p-Anisoyl)-2-ethyl-6-methoxy-benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | Tin tetrachloride | HCID 24287 | — |
| Reactant | 2-Ethyl-6-methoxy-1-benzofuran | HCID 22143600 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(p-Anisoyl)-2-ethyl-6-methoxy-benzofuran | HCID 52952047 | — |
Reaction Steps
Dried carbon disulfide solution (20 ml) of 2-ethyl-6-methoxy-benzofuran (2.76 g, 15.6 mmol) and p-anisoyl chloride (3.48 g, 20.3 mmol) was cooled on ice, to which tin chloride (IV) was dropped (5.25 g, 20.3 mmol) while stirring. The mixture was stirred at a temperature in a range of 5 to 10° C. for 3 hours and then poured into water. The organic layer was washed with diluted hydrochloric acid and water, dried over MgSO4, and concentrated under reduced pressure. Crude product thereof was purified by HPLC (silica gel, ethyl acetate: hexane=2:8) and a target product in pale yellow oily state (2.98 g, 9.60 mmol, 58%) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07521570B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-578cc6e4b3fe4120b4865e6cc81a9820 |
| Source note | uspto-grants-2009_04 |