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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654106Generated: November 3, 2026

Dimethyl Sulfoxide → 5-(Difluoromethyl)furan-2-carbaldehyde

https://huagongshe.com/reaction/1654106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantOxalyl chlorideHCID 65578—
Reactant(5-(Difluoromethyl)furan-2-yl)methanolHCID 20079677—
ReactantMonosodium phosphateHCID 23672064—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product5-(Difluoromethyl)furan-2-carbaldehydeHCID 2007963870.4%

Reaction Conditions

Temperature-60 °C

Reaction Steps

A solution of 6.5 ml of DMSO (dimethyl sulfoxide) and 60 ml of methylene chloride was added at -60° C. under a nitrogen atmosphere to a solution of 3.84 ml of oxalyl chloride and 40 ml of methylene chloride. The reaction mixture was stirred at -60° C. and 3.6 g of 5-difluoromethyl,2-furanmethanol in solution in 30 ml of methylene chloride were added. The mixture was stirred for 2 hours at -60° C. and a solution of 16.1 ml of triethylamine and 30 ml of methylene chloride was added over 15 minutes. The reaction mixture was stirred for half an hour at -60° C., the temperature was allowed to rise to -20° C. The mixture was stirred for half an hour at this temperature and then poured into a solution of sodium dihydrogenphosphate and extracted with methylene chloride. The extract was dried and the 3.6 g of product were chromatographed on silica by eluting with an 8/2 hexane/ethyl acetate mixture to obtain after chromatography, 2.5 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05405865
Source datasetuspto-grants-1995_04
ORD IDord-da217df111a54be78bd7dfb445597b71
Source noteuspto-grants-1995_04