HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → Diisopropylether hexane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 15670660 | HCID 15670660 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Diisopropylether hexane | HCID 21881879 | — |
Reaction Steps
A mixture of 5.0 g. (11.73 mmole) of trans-3-(2,4-dibenzyloxyphenyl)-4-(2-propenyl)cyclohexanone, 6.5 ml. (117 mmole) of ethylene glycol and 223 mg. (1.17 mmole) of p-toluenesulfonic acid in 50 ml. of benzene was heated at reflux for 1.5 hours. Water was removed via a soxhlet extractor filled with molecular sieves. The reaction was cooled and added to 500 ml. saturated sodium bicarbonate and 300 ml. ether. The ether phase was separated, dried over magnesium sulfate and evaporated. Trituration with diisopropyl ether-hexane gave 5.31 g. (96%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04831059 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-d9baf52537fe4f659fd7b847d8b9dd7b |
| Source note | uspto-grants-1989_05 |