HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanone, 1-(2,6,6-trimethyl-3-cyclohexen-1-yl)- → Trans-4-Acetyl-3,5,5-Trimethylcyclohexene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanone, 1-(2,6,6-trimethyl-3-cyclohexen-1-yl)- | HCID 117287 | — |
| Catalyst | Rhodium chloride trihydrate | HCID 11459718 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Trans-4-Acetyl-3,5,5-Trimethylcyclohexene | HCID 54437493 | — |
Reaction Steps
In a 200-ml four-necked flask equipped with a thermometer, condenser and a stirrer, placed were 2,6,6-trimethyl-3-cyclohexenyl methyl ketone (10 g) synthesized in Referential Example 1, ethyl alcohol (40 ml) and rhodium trichloride trihydrate (0.9 g). Under stirring, they were reacted at 90° C. for 24 hours. The reaction mixture at this time was sampled and analyzed by gas chromatography, resulting in that the content of trans-2,6,6-trimethyl-3-cyclohexenyl methyl ketone was 11%, while those of 2,6,6-trimethyl-2-cyclohexenyl methyl ketone and 2,6,6-trimethyl-1-cyclohexenyl methyl ketone produced by the above reaction were 87% and 2%, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06822121B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-0e4410c17a534a3fab617a724f481df4 |
| Source note | uspto-grants-2004_11 |