Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,3-Dichloro-5,5-dimethylpiperidin-2-oneHCID 21941387—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
Product3-Chloro-5,5-dimethylpiperidin-2-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812014B2
Source datasetuspto-grants-2010_10
ORD IDord-34b5b84805e4429ba52c5ddc8b8731cd
Source noteuspto-grants-2010_10