HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → Ethyl(6-chloro-1-benzofuran-3-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Carboxymethylene triphenylphosphorane | HCID 10870911 | — |
| Reactant | 6-Chloro-3-Benzofuranone | HCID 13778133 | — |
| Product | Ethyl(6-chloro-1-benzofuran-3-yl)acetate | HCID 12936152 | — |
Reaction Steps
A mixture of 6-chloro-benzofuran-3 (2H)-one (1.68 g, 10 mmol) and (carboxymethylene)triphenylphosphorane (5.22 g, 15 mmol) was refluxed in toluene (100 ml) for 48 hrs. At the end, the reaction mixture was concentrated and loaded over a silica-gel column. The column was eluted with hexane (500 ml) and later with 25% ethyl acetate. The product, ethyl(6-chloro-1-benzofuran-3-yl)acetate, was obtained as a white oil. Yield: 2.1 g (87%); 239 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07235569B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-610e968e9bc84b3694fa106934be9194 |
| Source note | uspto-grants-2007_06 |