HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172194Generated: October 31, 2026
1,4-Cyclohexanedione → HCID 70873346, compound
https://huagongshe.com/reaction/2172194
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Cyclohexanedione | HCID 12511 | — |
| Reactant | 4-(3,4-Dichlorophenoxy)piperidine | HCID 3732042 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 70873346 | HCID 70873346 | 53.3% |
Reaction Steps
10% palladium on carbon (350 mg) was added to an ethanol solution (50 ml) of 4-(3,4-dichlorophenoxy)piperidine (7.1 g) and 1,4-cyclohexanedione (6.47 g), and the mixture was stirred at 50 to 60° C. for 5 hours. After being cooled to room temperature, the catalyst was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was dissolved in ethyl acetate, 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=9:1→3:1) to afford the title compound as a pale brown powder (5.2 g).
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-822f3477d8f94f88800a621ba63096a9 |
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| Source note | uspto-grants-2015_06 |
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