HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 5-Bromo-1,1-(ethylenedioxo)-indane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Ammonia | HCID 222 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 5-Bromo-1-indanone | HCID 520695 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 5-Bromo-1,1-(ethylenedioxo)-indane | HCID 45158894 | — |
Reaction Steps
A mixture of 5-bromo-1-indanone (13.0 g, 61.8 mmol), p-toluenesulfonic acid (23 mg, 0.12 mmol) and ethylene glycol (27.6 mL, 494.6 mmol) in benzene (140 mL) was refluxed for about 24 hours, using a Dean-Stark trap to remove water. The mixture was cooled, poured into excess 5% aqueous sodium bicarbonate and was extracted with toluene. The combined organic extracts were washed with brine, dried with MgSO4, filtered, and evaporated in vacuum. The residue was purified by flash column chromatography using dichloromethane as the mobile phase to give the above intermediate. MS (DCI/NH3): m/z 254, 256 (M)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07320986B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-89f48ed5b59a4f4195cf5a3d58126f1e |
| Source note | uspto-grants-2008_01 |