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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769734Generated: October 29, 2026

Dimethyl Sulfoxide → 1-(Cyclopropanecarbonyl)piperidin-4-one

https://huagongshe.com/reaction/1769734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant1-Cyclopropanecarbonyl-4-hydroxypiperidineHCID 14994967—
SolventDichloromethaneHCID 6344—
Solvent1,1-DichloroethaneHCID 6365—
Product1-(Cyclopropanecarbonyl)piperidin-4-oneHCID 1499496876%

Reaction Steps

66 g of oxalic chloride was dissolved in 500 ml of dichloroethane, into which 61 g of dimethyl sulfoxide was gradually dropped at -67° C. 44 g of 1-cyclopropanecarbonyl-4-hydroxypiperidine dissolved in 200 ml of dichloromethane was dropped into the above solution at -67° C. At -67° C., 131 g of triethylamine was further added, followed by returning to room temperature. The resultant salt was removed by filtration and the filtrate was once concentrated, after which water was added to the concentrate, followed by extraction with ethyl acetate and drying with anhydrous magnesium sulfate. Moreover, the aqueous phase was extracted with chloroform and dried similarly. The solvent was distilled off under reduced pressure and the resultant residue was purified by the use of silica gel column chromatography (elution solvent: ethyl acetate:hexane=3.7), thereby obtaining 33 g of the intended compound (yield 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05382579
Source datasetuspto-grants-1995_01
ORD IDord-81fd69bcd6844f8985fd56a68bc4e405
Source noteuspto-grants-1995_01