HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → 2-Cyclohexen-1-one, 2,5,6-trimethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Ethyl ketone | HCID 7288 | — |
| Reactant | 3-Hydroxybutanal | HCID 7897 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Cyclohexen-1-one, 2,5,6-trimethyl- | HCID 89264 | 47.1% |
Reaction Steps
A mixture of 88 g of β-hydroxybutyraldehyde and 150 g of diethyl ketone is added dropwise in the course of one hour to a mixture of 250 g of diethyl ketone, 80 g of isopropanol and 5 g of sodium hydroxide powder which is boiling under reflux. The whole is boiled for another hour under reflux. Neutralization is effected with glacial acetic acid and the aqueous phase is separated. The organic layer is fractionated. 65 g of 2,5,6-trimethyl-2-cyclohexen-1-one having a boiling point of 74° to 76° C. at 12 mm Hg is obtained. The yield is 47% with reference to β-hydroxybutyraldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04128728 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-c16defd56be34a8fba979fa521f18f93 |
| Source note | uspto-grants-1978_12 |