HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ketoisophorone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Isophorone | HCID 6544 | — |
| Catalyst | Copper Sulfate | HCID 24462 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Ketoisophorone | HCID 62374 | — |
Reaction Steps
A 1-1 three-neck flask equipped with a gas inlet frit, a stirrer and an intensive condenser was charged with 350 ml of toluene, 350 g of isophorone, 11.4 g of H3 [P(Mo3O10)4 ]×H2O, 1.4 g of CuSO4 ·5H2O and 1.4 g of MoO3. After compressed air had been passed through at 110° C. for 90 hours, the reaction mixture was added a little at a time at 80° C. into 4 1 of boiling n-hexane. The mixture was then filtered, and the filtrate was concentrated in a rotary evaporator. The yellowish oil obtained by distillation at 97° C./13 mbar was converted into almost colorless crystals at -18° C. by addition of 10% by volume of n-hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05101032 |
| Source dataset | uspto-grants-1992_03 |
| ORD ID | ord-3a3c1ed0243d41f297a97f0fa0951655 |
| Source note | uspto-grants-1992_03 |