HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → HCID 21459585, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 21459573 | HCID 21459573 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 21459585 | HCID 21459585 | — |
Reaction Steps
2 g (5.12 mmol) of the ketone obtained in Example 8, in 20 ml of benzene, were treated with 0.5 ml of ethylene glycol and 10 mg of TsOH. The reaction mixture was heated at reflux for 24 hours and was then neutralized with a saturated sodium bicarbonate solution. After extraction with ethyl ether, the organic phase was washed with water, dried over magnesium sulfate, filtered and evaporated to yield, after chromatography on silica in a hexane/EtOAc (90/10) mixture and triturating in hexane, 910 mg (41%) of the expected compound, melting at 136°-137° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05702710 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-c2063b01413c46a39337f710a375eff1 |
| Source note | uspto-grants-1997_12 |