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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031866Generated: October 26, 2026

Dimethyl Sulfoxide → 2-(2,4-Dichlorophenoxy)propanal

https://huagongshe.com/reaction/1031866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant2-(2,4-Dichlorophenoxy)propan-1-olHCID 350983—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-(2,4-Dichlorophenoxy)propanalHCID 2216635922.1%

Reaction Conditions

Temperature-60 °C

Reaction Steps

4.68 g of DMSO were added under nitrogen to a stirred solution of 3.81 g of oxalyl chloride in 75 ml of methylene chloride at -60° C. to -50° C. After 2 minutes a solution of 6.4 g of 2-(2,4-dichlorophenoxy)propanol in 40 ml of methylene chloride was added. The mixture was stirred at -60° C. for a further 15 minutes and was then treated with 13.7 g of triethylamine After a further 5 minutes at -60° C. the mixture was allowed to warm to room temperature. 150 ml of water were added and the layers were separated. The aqueous layer was extracted with 150 ml of methylene chloride and the combined organic extracts were washed successively with sodium chloride solution, dilute hydrochloric acid, water, dilute sodium carbonate solution and water, dried over sodium sulphate and evaporated. The residue was purified by chromatography on silica gel using ethyl acetate/n-hexane (1:4) for the elution. There were obtained 1.4 g of 2-(2,4-dichlorophenoxy)propionaldehyde, mp 87°-88° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04956346
Source datasetuspto-grants-1990_09
ORD IDord-77081c33126346a896356205fcf11eb7
Source noteuspto-grants-1990_09