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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446583Generated: October 26, 2026

Dimethyl Sulfoxide → 1-(4-Fluoro-3-methoxyphenyl)ethanone

https://huagongshe.com/reaction/1446583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant1-(4-Fluoro-3-methoxyphenyl)ethan-1-olHCID 24721520—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-(4-Fluoro-3-methoxyphenyl)ethanoneHCID 277453298.9%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of dimethyl sulfoxide (1.33 mL) in dichloromethane (5 mL) was added dropwise to a solution of oxalyl chloride (1.63 mL) in dichloromethane (80 mL) in a nitrogen atmosphere at −78° C. After stirring the reaction solution at −78° C. for 3 minutes, a solution of 1-(4-fluoro-3-methoxyphenyl)ethanol (2.6 g) in dichloromethane (15 mL) was added dropwises to the reaction solution. Further, the reaction solution was stirred at −78° C. for 20 minutes, and triethylamine (10.8 mL) was added dropwise to the reaction solution. Then, the reaction solution was stirred at −78° C. for 10 minutes, and further stirred at room temperature for 30 minutes. Water and dichloromethane were added to the reaction solution and the organic layer was partitioned. The resulting organic layer was dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent:heptane-ethyl acetate system) to obtain 2.54 g of the title compound. The physical properties of the compound are as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07667041B2
Source datasetuspto-grants-2010_02
ORD IDord-081bdbf136c44db585c7dc6f2d98d825
Source noteuspto-grants-2010_02