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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269229Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 22493624, compound

https://huagongshe.com/reaction/2269229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 22493589HCID 22493589—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 22493624HCID 2249362494.8%

Reaction Steps

A solution of 923 μl of dimethyisulfoxide in 2 ml of dichloromethane was added dropwise to a solution of 797 pl of oxalyl chloride in 6 ml of dichloromethane at −60° C. under a nitrogen gas stream, followed by stirring for 5 minutes. To the reaction mixture, a solution of 1 g of 5,6,7,8-tetrahydro-3,5,5,8,8-pentamethylquinoxaline-2-methanol in 6 ml of dichloromethane was added dropwise and the resulting mixture was stirred for 15 minutes. Triethylamine (4.8 ml) was then added dropwise to the reaction mixture, followed by stirring for 5 minutes. After the reaction mixture was raised to room temperature and stirred for 15 minutes, water was added thereto. The resulting mixture was extracted with dichloromethane. The organic layer was successively washed with water and saturated saline, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue so obtained was subjected to chromatography on a silica gel column (developing solvent: 10% ethyl acetate/n-hexane), whereby 940 mg of the title compound were obtained in the form of a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329402B1
Source datasetuspto-grants-2001_12
ORD IDord-23ed626dc13e4abeb88f91e4644b3522
Source noteuspto-grants-2001_12