HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl ketone → 2-Cyclohexen-1-one, 2,5,6-trimethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl ketone | HCID 7288 | — |
| Reactant | 3-Methoxybutyraldehyde | HCID 98040 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Cyclohexen-1-one, 2,5,6-trimethyl- | HCID 89264 | 56% |
Reaction Steps
102 g of β-methoxybutyraldehyde is dripped in the course of one hour into a mixture of 500 g of diethyl ketone and 10 g of a 30% solution of sodium methylate in methanol which is boiling under reflux. The whole is then heated for another hour under reflux. The reaction mixture is processed as described in Example 2. 77 g of 2,5,6-trimethyl-2-cyclohexen-1-one is obtained, i.e. a 56% yield with reference to β-methoxybutyraldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04128728 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-9c14c87cead5429790577056f90c7ce5 |
| Source note | uspto-grants-1978_12 |