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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476844Generated: October 25, 2026

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

https://huagongshe.com/reaction/476844

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 numberUS04886785
Source datasetuspto-grants-1989_12
ORD IDord-6bbe6b5ead9c42a59d208ecb2cb25c51
Source noteuspto-grants-1989_12