HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172186Generated: October 31, 2026
1,4-Cyclohexanedione → HCID 67275119, compound
https://huagongshe.com/reaction/2172186
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Cyclohexanedione | HCID 12511 | — |
| Reactant | HCID 23081575 | HCID 23081575 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67275119 | HCID 67275119 | 17.6% |
Reaction Steps
10% palladium on carbon (64 mg) was added to an ethanol solution (13 ml) of 4-(4-trifluoromethoxybenzyl)piperidine (1.28 g) and 1,4-cyclohexanedione (1.19 g), and the mixture was stirred at 70 to 80° C. for 8.5 hours. After being cooled to room temperature, the catalyst was removed by filtration, and the filtrate was concentrated under reduced pressure. After being dissolved in ethyl acetate, the residue was washed with a saturated sodium chloride aqueous solution and dried over magnesium sulfate. After being concentrated under reduced pressure, the residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:0→6:4) to afford the title compound as a black oil (305 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051333B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-cf96a904f7bc4cee9e8328e307e9cf53 |
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| Source note | uspto-grants-2015_06 |
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