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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971122Generated: October 31, 2026

Dimethyl Sulfoxide → HCID 59021633, compound

https://huagongshe.com/reaction/971122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 59021630HCID 59021630—
SolventDichloromethaneHCID 6344—
ProductHCID 59021633HCID 59021633100.2%

Reaction Steps

To a stirred solution of 36 ml oxalyl chloride (0.42 mol; Fluka) in 1100 ml dichloromethane were added at −70° C. a solution of 44 ml dimethyl sulfoxide (0.62 mol) in 800 ml dichloromethane over 0.5 h. After stirring at −700 for 15 min a solution of 77.5 g N-benzyl-N-methyl-isoleucinol (0.35 mol) in 700 ml dichloromethane was added at −70° C. over ˜0.5 h and stirring was continued for 15 min. After the addition of 234 ml triethylamine (1.68 mol) at −65° C. stirring was continued for 5 min and the white suspension stirred at −50° C. for 1 h. The dry ice-bath was removed and 3000 ml deionized water was added drop wise and under stirring while the reaction mixture was warmed up to RT. The organic layer was washed twice with 2000 ml 10% brine and the organic layer was dried (Na2SO4). Removal of the solvent by rotary evaporation (40° C./≧10 mbar/0.1 mbar, 2 h) yielded 76.9 g (100.2%) yellow oily product which was used without purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312343B2
Source datasetuspto-grants-2007_12
ORD IDord-f7a16f48105e48c88fda015c3548724a
Source noteuspto-grants-2007_12