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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941280Generated: November 2, 2026

Dimethyl Sulfoxide → HCID 21221318, compound

https://huagongshe.com/reaction/1941280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 21221403HCID 21221403—
SolventDichloromethaneHCID 6344—
ProductHCID 21221318HCID 2122131873.3%

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a solution of oxalyl chloride (1.26 ml) in methylene chloride (30 ml) at -70° C., a solution of dimethylsulfoxide (2.11 ml) in methylene chloride (3.0 ml) was added dropwise. To the obtained solution, a solution of methyl 3-(4-hydroxybutyl)phenoxyacetate (1.94 g) in methylene chloride (8.0 ml) was added dropwise. Triethylamine (6.9 ml) was added dropwise thereto while the reaction temperature was maintained at -70° C. The reaction mixture was warmed slowly to -40° C. over a 30 min period and then quenched by addition of a saturated aqueous solution of ammonium chloride. The reaction mixture was extracted with ether. The extract was washed with a saturated aqueous solution of ammonium chloride and a saturated aqueous solution of sodium chloride, successively, dried over anhydrous magnesium sulfate and evaporated. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=5:2) to give the title compound (1.41 g) having the following physical data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05703099
Source datasetuspto-grants-1997_12
ORD IDord-21021df3aff140d194a6b25fb200d8c8
Source noteuspto-grants-1997_12