HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129502Generated: October 29, 2026
Dimethyl Sulfoxide → 1-(Cyclopropanecarbonyl)piperidin-4-one
https://huagongshe.com/reaction/129502
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(Cyclopropanecarbonyl)piperidin-4-one | HCID 14994968 | 76% |
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-cycloprpanecarbonyl-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 reside 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05468740 |
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| Source dataset | uspto-grants-1995_11 |
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| ORD ID | ord-ed99b4b9ee0346ff84d4dcd6928e88df |
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| Source note | uspto-grants-1995_11 |
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