HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374802Generated: October 29, 2026
Dimethyl Sulfoxide → HCID 15665591, compound
https://huagongshe.com/reaction/374802
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 15665590 | HCID 15665590 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15665591 | HCID 15665591 | 87.3% |
Reaction Steps
25 ml of oxalyl chloride was added to 500 ml of dichloromethane, into which 41 ml of dimethyl sulfoxide was gradually dropped in a stream of nitrogen at a temperature of from -50° C. to -70° C. Subsequently, 10.3 g of N-(3-butynyloxycarbonyl)-4-hydroxypiperidine was dissolved in 50 ml of dichloromethane, followed by gradually dropping into the reaction mixture. Finally, 120 ml of triethylamine was dropped, followed by gradually increasing the temperature up to room temperature. The reaction solution was charged into a saturated saline solution, extracted three times with dichloromethane and dried with anhydrous magnesium sulfate, after which the solvent was distilled off under reduced pressure. The resultant residue was purified by the use of silica gel column chromatography (elution solvent: hexane:ethyl acetate=3.1), thereby obtaining 8.9 g of the intended compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05482937 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-f7452d85324747cc8154c41921e25345 |
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| Source note | uspto-grants-1996_01 |
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