HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → HCID 18690801, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 18350561 | HCID 18350561 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | HCID 18690801 | HCID 18690801 | — |
Reaction Steps
A mixture of 5-tert-butyl-2-indancarbaldehyde (ex. 4; 9.8mmole), ethyleneglycol (6.1 g, 98 mmole) and p-toluenesulfonic acid (95 mg, 0.5 mmole) in cyclohexane (25 ml), was heated to reflux (80°) during 3 h with a Dean-Stark type trap. The cooled mixture was poured on ether and aq. sat. NaHCO3, and the organic phase was washed with aq. sat. NaHCO3, dried over K2CO3 and concentrated. After bulb-to-bulb distillation, the desired dioxolane was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05552379 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-e40453907c9c4273b7e73c90285edd2b |
| Source note | uspto-grants-1996_09 |