HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → HCID 178448011, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-Buten-2-one, 3-(trimethylsilyl)- | HCID 10997141 | — |
| Reactant | HCID 86744107 | HCID 86744107 | — |
| Reactant | HCID 178448028 | HCID 178448028 | — |
| Reactant | HCID 178448061 | HCID 178448061 | — |
| Catalyst | Calcium Palladium Carbonate | HCID 12000666 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178448011 | HCID 178448011 | — |
Reaction Steps
A solution of 6.5 g of 3-[trans-4-(trans-4-n-propyl-cyclohexyl)-cyclohexyl]-cyclohex-2-enone [m.p. 96.5°; obtainable by reacting trans-4-(trans-4-n-propycyclohexyl)-acetylcyclohexane with LDA/ether at -85°, adding 1-(trimethylsilyl)-vinyl methyl ketone at -95°, allowing the mixture to warm up to room temperature, adding methanolic KOH and working up in the customary manner (silica gel; 5:3.5:1.5 petroleum ether:methylene chloride:ether)] in 210 ml of ethanol is added to a suspension of 1.7 g of 5% Pd/CaCO3 in 75 ml of ethanol, and the mixture is stirred under hydrogen for 2 hours. Removing the catalyst and working up in the customary manner gives 3-[trans-4-(trans-4-n-propylcyclohexyl)-cyclohexyl]-cyclohexanone, m.p. 1.5°, c.p. 158.2°
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04943384 |
| Source dataset | uspto-grants-1990_07 |
| ORD ID | ord-42553f418e204eda8254a55455ee383e |
| Source note | uspto-grants-1990_07 |