HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → HCID 12596328, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 1,9-Cyclohexadecanedione | HCID 11345773 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 12596328 | HCID 12596328 | — |
Reaction Steps
To a solution of 44.0 g (175 mmol) of 1,9-cyclohexadecanedione in 125 ml of toluene is added 13.1 g (210 mmol) of ethylene glycol and 500 mg (2.5 mmol) of p-toluenesulphonic acid. The mixture is then heated with a water separator until visible amounts of water are no longer eliminated. Washing with sat. NaHCO3 solution is then carried out, the phases are separated, the organic phase is dried over Na2SO4, filtration is carried out, and the solvent is removed on a rotary evaporator. This gives 57.7 g of a solid comprising 3 components having the following GC content: 1,9-cyclohexadecanedione (33.7%); 1,4-dioxaspiro-[4.15]-eicosan-13-one (52.5%); 1,4,14,17-tetraoxadispiro-[4.7.4.7]-tetracosane (13.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06815413B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-0c0cb7922e144bc7a0eaa50f0b0636f8 |
| Source note | uspto-grants-2004_11 |