HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → Ethyl(5-chloro-1-benzofuran-3-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 5-Chloro-2,3-dihydro-1-benzofuran-3-one | HCID 3711352 | — |
| Reactant | Carboxymethylene triphenylphosphorane | HCID 10870911 | — |
| Product | Ethyl(5-chloro-1-benzofuran-3-yl)acetate | HCID 12936153 | — |
Reaction Steps
A mixture of 5-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, 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(5-chloro-1-benzofuran-3-yl)acetate, was obtained as a white oil. Yield: 1.8 g (75%); 239 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07235569B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-2aaccd3a2d09422f82c582d31508503a |
| Source note | uspto-grants-2007_06 |