HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethyl phosphonoacetate → Methyl Benzofuran-3-acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethyl phosphonoacetate | HCID 13345 | — |
| Reactant | Coumaranone | HCID 23556 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Oxygen | HCID 977 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl Benzofuran-3-acetate | HCID 10976279 | — |
Reaction Steps
KOtBu (0.673 g, 6 mmol) was dissolved in dry DMF (10 ml) with exclusion of oxygen. Phosphonoacetic acid triethyl ester (0.87 ml, 6 mmol) was then added to the mixture. After 20 min a solution of benzofuran-3(2H)-one (0.536 g, 4 mmol) in dry DMF (10 ml, argon atmosphere) was added to this mixture. The reaction mixture was stirred at room temperature for 1 h and thereafter poured on to ice (50 ml) for working up. The mixture obtained was extracted with diethyl ether (4×20 ml). The organic phase was washed with water (4×20 ml), dried with Na2SO4 and then concentrated. The product formed was purified by column chromatography [silica gel 60 (50 g); cyclohexane, ethyl acetate (4:1)] and obtained in a yield of 0.372 g (48%) as a yellowish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08138187B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-59d2d9c549a0457c91d3ff58936a4e86 |
| Source note | uspto-grants-2012_03 |