HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158895Generated: October 31, 2026
3,3-Dichloro-5,5-dimethylpiperidin-2-one → 3-Chloro-5,5-dimethylpiperidin-2-one
https://huagongshe.com/reaction/1158895
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,3-Dichloro-5,5-dimethylpiperidin-2-one | HCID 21941387 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Chloro-5,5-dimethylpiperidin-2-one | HCID 21941379 | — |
Reaction Steps
To 40.8 g (0.21 mol) of 3,3-dichloro-5,5-dimethyl-2-piperidone dissolved in 410 mL of AcOH was added 10% Pd/C (50% wet, 6.2 g) and NaOAc-3H2O (62.4 g, 0.46 mol) and the mixture was hydrogenated at 300 kPa for 20 min. The pressure of hydrogen was adjusted at 300 kPa every 5 min. The catalyst was removed by filtration and the filtrate concentrated under reduced pressure. CHCl3 (400 mL) and water (300 mL) were added to the residue and the aqueous layer was neutralized with 4 mol/L NaOH. The mixture was separated and the aqueous layer was extracted with CHCl3 (5×300 mL) and the organic layer was dried (MgSO4) and filtered. The filtrate was concentrated under reduced pressure. The residue was applied to silica-gel column chromatography, and then the column was eluted with hexane-AcOEt (1:1). The titled compound was obtained as a white solid (20.4 g, 59.9%). (J. Med. Chem., 20, 1176 (1977))
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07812014B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-34b5b84805e4429ba52c5ddc8b8731cd |
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| Source note | uspto-grants-2010_10 |
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