HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 22844417, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Methyl vinyl ketone | HCID 6570 | — |
| Reactant | HCID 57294670 | HCID 57294670 | — |
| Reactant | HCID 178418582 | HCID 178418582 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22844417 | HCID 22844417 | — |
Reaction Steps
This compound was prepared by aldol condensation of 2 g (0.011 mol) of (+)-(1R,5S)-5-ethyl-2,6,6-trimethyl-2-cyclohexen-1-carbaldehyde (obtained according to example 4i.) with 2 ml (0.03 mol) of acetone, in 10 ml of ethanol. After adding 0.1 ml of a 30% solution of CH3ONa in methanol, the reaction was allowed to proceed for about 65 h. Following the usual treatment, 1.3 g of 95% pure mixture were obtained, containing 83% of the above-mentioned butenone, 13% of its α-trans isomer and 4% of its α-cis isomer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05118865 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-78b2726e3119468884b95930392f9853 |
| Source note | uspto-grants-1992_06 |