HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethoxymethane → HCID 18351832, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethoxymethane | HCID 8020 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 18351576 | HCID 18351576 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18351832 | HCID 18351832 | 58% |
Reaction Steps
2,3-dihydro-2-hydroxymethyl-3-oxo-7-methoxybenzofuran (1.79 g) and dimethoxymethane (10 ml) were dissolved in dichloromethane (25 ml) and phosphorus pentoxide (3.47 g) was added to the obtained solution, followed by stirring the resulting solution at room temperature for 3.5 hours. The reaction mixture was added to saturated aqueous sodium hydrogen carbonate solution and extracted with ethyl acetate. The organic layers were combined and washed with water and with saturated brine, followed by drying over magnesium sulfate. Magnesium sulfate was removed by filtration and the solvent was evaporated off. The residue was purified by column chromatography (solvent: n-hexane/ethyl acetate=1/1) to obtain the desired compound (912 mg, yield: 58%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06323235B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-86e783baf43741129f9fbee3fc309a9a |
| Source note | uspto-grants-2001_11 |