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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556522Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 59000932, compound

https://huagongshe.com/reaction/556522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 59000874HCID 59000874—
SolventDichloromethaneHCID 6344—
ProductHCID 59000932HCID 5900093213.2%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of oxalyl chloride (0.20 g, 1.58 mmol) in dichloromethane (2 ml) was dropwise added a solution of dimethylsulfoxide (163 mg, 2.09 mmol) in dichloromethane (2 ml) under cooling at −78° C. After stirring for 10 minutes, a solution of the compound (308 mg, 0.5 mmol) obtained in Example 61 in dichloromethane (2 ml) was dropwise added. After stirring for further 30 minutes, triethylamine (0.40 ml, 2.88 mmol) was dropwise added, and the mixture was stirred at 0° C. for 2 hours. To the mixture was added an aqueous solution of ammonium chloride at 0° C., and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and concentrated with under reduced pressure. The residue was purified by NH-silica gel (Produced by Fuji Silysia Chemical Ltd.) column chromatography (eluent; ethyl acetate), and the obtained powders was washed with diisopropyl ether and hexane to give the title compound (40.7 mg, 13%) as pale yellow powders.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058280B2
Source datasetuspto-grants-2011_11
ORD IDord-73706b546f264b88bae4854c2f04ae74
Source noteuspto-grants-2011_11