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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820639Generated: October 29, 2026

Dimethyl Sulfoxide → HCID 58847106, compound

https://huagongshe.com/reaction/1820639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantHydrogen PeroxideHCID 784—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 58847064HCID 58847064—
SolventAcetoneHCID 180—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 58847106HCID 5884710653.4%

Reaction Steps

A solution of 4-(cis-2,6-dimethylmorpholin-4-yl)-3-formylbenzonitrile (Example 6, Step 1) (0.244 g, 1.00 mmol) in acetone (4 mL) is treated with anhydrous powdered potassium carbonate (0.028 g, 0.20 mmol) followed by 30% hydrogen peroxide (0.204 g, 6.00 mmol).The reaction mixture is stirred at room temperature. After 24 h, additional 30% hydrogen peroxide (6.0 mmol) and acetone (2 mL) is added. After stirring at RT for 5 days, an additional potassium carbonate (0.96 g) and DMSO (4 mL) is added and stirred at RT for 24 h. The reaction mixture is poured into 50% saturated brine (40 mL), extracted with ether (3×), dried (NaSO4) and concentrated. The resulting residue is purified by silica gel chromatography using acetone-methylene chloride (1:4) as the eluent, to afford 28 mg (11%) of the desired amide as a yellow foam. 1H NMR (400 MHz, CDCl3) δ 10.20, 8.20, 8.09, 7.12, 6.47-5.88, 4.00-3.86, 3.20, 2.74, 1.25.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605157B2
Source datasetuspto-grants-2009_10
ORD IDord-0aff73aa1be44d8b90ba4fe3e8a964bb
Source noteuspto-grants-2009_10