Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807906Generated: October 30, 2026

Dimethyl Sulfoxide → 2-(4-Fluorophenyl)-2-methylpropanal

https://huagongshe.com/reaction/1807906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant2-(4-Fluorophenyl)-2-methylpropan-1-olHCID 21262802—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-(4-Fluorophenyl)-2-methylpropanalHCID 82074750—

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a stirred solution of oxalyl chloride (2.81 ml) in dichoromethane (30 ml) at −60° C. was added dropwise a solution of dry dimethyl sulphoxide (4.84 ml) in dichloromethane (20 ml). The mixture was stirred for 15 min at −60° C. and then a solution of 2-(4-fluoro-phenyl)-2-methyl-propan-1-ol (4.59 g; CAS 703-10-6) in dichloromethane (20 ml) was added dropwise. The mixture was stirred at −60° C. for 2 hours and then triethylamine (18.9 ml) was added dropwise. The reaction mixture was allowed to warm to room temperature and diluted with water and with dichloromethane. The phases were separated and the organic phase was washed with water and then dried over Na2SO4 and concentrated in vacuo. The residue was purified by column chromatography (SiO2, heptane/EtOAc gradient) to yield a colourless oil, (3.47 g, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357712B2
Source datasetuspto-grants-2013_01
ORD IDord-fb928b76fc3b413d964918a05317227a
Source noteuspto-grants-2013_01