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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165015Generated: October 31, 2026

Dimethyl Sulfoxide → 3-Chloro-2-methoxymethoxy-2'-methoxymethoxybenzophenone

https://huagongshe.com/reaction/2165015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant(3-Chloro-2-methoxymethoxyphenyl)(2-methoxymethoxyphenyl)methanolHCID 19812669—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product3-Chloro-2-methoxymethoxy-2'-methoxymethoxybenzophenoneHCID 1981267299.6%

Reaction Steps

A solution of 16.0 ml of oxalyl chloride in 500 ml of dichloromethane was placed in a 1 l flask and cooled with a dry ice-acetone bath. Dimethyl sulfoxide (14.0 ml) was added dropwise with stirring over a 10 min period. After a 40 min reaction period, a solution of 51.0 g of (3-chloro-2-methoxymethoxyphenyl)(2-methoxymethoxyphenyl)methanol in 120 ml of dichloromethane was added dropwise over a 45 min period with stirring at about -78° C. and allowed to react another 45 min. An orange suspension formed. Triethylamine (50 ml) was added and the slurry was swirled occasionally and was allowed to warm to room temperature. The slurry was diluted with 1 l of ether and the resulting mixture was extracted with 3-300 ml portions of water, 300 ml of 2 percent hydrochloric acid, and 200 ml of saturated aqueous sodium bicarbonate, dried over magnesium sulfate, filtered, and concentrated by evaporation under reduced pressure to obtain 50.5 g of the title compound as a viscous pale orange-tinted oil. The proton and carbon NMR spectra were consistent with the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04938790
Source datasetuspto-grants-1990_07
ORD IDord-d3e2b05d02db40c995e6abdb4cc2df18
Source noteuspto-grants-1990_07