HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → HCID 12337274, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | 3-Bromo-1-benzofuran-2-carbaldehyde | HCID 12337272 | — |
| Catalyst | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 12337274 | HCID 12337274 | 100.5% |
Reaction Steps
3-bromo-1-benzofuran-2-carbaldehyde (5.49 g, 24.4 mmol) is combined with para-toluene sulfonic acid hydrate (232 mg, 1.2 mmol) and ethylene glycol (2.44 ml, 43.9 mmol) in benzene (75 ml). The reaction is refluxed with a Dean-Stark trap for 5 h. The mixture is cooled to rt and diluted with saturated NaHCO3 solution (20 ml) and left to stir for an additional 12 h. The layers are allowed to separate, and the organic layer is dried over Na2SO4, filtered, and concentrated to afford 6.6 g (100%) of 3-bromo-2-(1,3-dioxolan-2-yl)-1-benzofuran as a dark brown oil. HRMS (FAB) calcd for C11H9BrO3+H: 268.9814, found 268.9821.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07067515B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-8afef1419604449ea0fc31f051252fd0 |
| Source note | uspto-grants-2006_06 |