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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374802Generated: October 29, 2026

Dimethyl Sulfoxide → HCID 15665591, compound

https://huagongshe.com/reaction/374802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 15665590HCID 15665590—
SolventDichloromethaneHCID 6344—
ProductHCID 15665591HCID 1566559187.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05482937
Source datasetuspto-grants-1996_01
ORD IDord-f7452d85324747cc8154c41921e25345
Source noteuspto-grants-1996_01