HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 3-(4-(4-propylcyclohexyl)cyclohexyl)-2E-propenal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 4-(4-Propylcyclohexyl)cyclohexane | HCID 17884097 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 3-(4-(4-propylcyclohexyl)cyclohexyl)-2E-propenal | HCID 12020437 | — |
Reaction Steps
The resulting cyclohexane derivative was dissolved in a mixed solvent of acetone (80 ml) with 2N hydrochloric acid (8 ml), followed by heating the solution under reflux for 4 hours, cooling the reaction mixture down to room temperature after completion of the stirring, adding water, extracting with ether (50 ml), drying the organic layer over anhydrous magnesium sulfate, and concentrating under reduced pressure to obtain 3-(4-(4-propylcyclohexyl)cyclohexyl)-2E-propenal (3.1 g, 12 mmols). This product was used in the subsequent reaction without any purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05609791 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-9dbfd414898e43d9a8b53d0dcb76ce15 |
| Source note | uspto-grants-1997_03 |