HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → Cyclohexanone, 4-[(tetrahydro-2H-pyran-2-yl)oxy]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | 4-Hydroxycyclohexanone | HCID 543706 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Cyclohexanone, 4-[(tetrahydro-2H-pyran-2-yl)oxy]- | HCID 10012971 | — |
Reaction Steps
A solution comprising 10 g. of 4-hydroxycyclohexanone, 10 g. of dihydropyran and 0.5 g. of p-toluenesulfonic acid in 100 ml. of ether is allowed to stand at room temperature for about 2.5 hours. The solution is then washed with saturated aqueous sodium bicarbonate solution and brine, 50 ml. of dry benzene added and the solution then evaporated to dryness to give 4-[(tetrahydropyran-2-yl)oxy]cyclohexanone as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03960961 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-03f6c97d89e84219b6c210a65545ae43 |
| Source note | uspto-grants-1976_06 |