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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264110Generated: November 1, 2026

Dimethyl Sulfoxide → HCID 21469481, compound

https://huagongshe.com/reaction/264110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 21469489HCID 21469489—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 21469481HCID 21469481—

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a cold (-60° C.), stirred solution of oxalyl chloride (32 mL, 0.37 mol) in dichloromethane (980 mL) was added over 10 minutes a solution of dimethylsulfoxide (52 mL, 0.73 mol) in CH2Cl2 (450 mL). Stirred 2 minutes. To the mixture was added a solution of (±)-2-hydroxy-1-phenyl-4-hexadecanone (105.6 g, 0.3176 mol) in CH2Cl2 (900 mL) over 17 minutes. Stirred 20 minutes. To the mixture was added triethylamine (230 mL, 1.65 mol) over 5 minutes. Stirred 5 minutes. The mixture was allowed to warm to -20° C. and water (1 L) was added. Stirred 30 minutes. The organic layer was washed (1M HCl and saturated NaCl), dried (Na2SO4), and rotoevaporated to an oil. The oil was chromatographed on silica gel using petroleum ether-acetone (45:1) to give a pale yellow oil; yield 67.6 g (64.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646170
Source datasetuspto-grants-1997_07
ORD IDord-e474694572cd44978f85136f986c97d9
Source noteuspto-grants-1997_07