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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390989Generated: October 29, 2026

Water → Flupyradifurone

https://huagongshe.com/reaction/2390989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
ReactantButyronitrileHCID 8008—
ReactantPotassium bisulfateHCID 516920—
ReactantN-[(6-chloropyridin-3-yl)methyl]-2,2-difluoroethanamineHCID 44604123—
ProductFlupyradifuroneHCID 1675277291%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a suspension of 5 g of sodium 4-(methoxycarbonyl)-5-oxo-2,5-dihydrofuran-3-oxide and 4.2 g of N-[(6-chloropyridin-3-yl)methyl]-2,2-difluoroethylamine in 35 ml of butyronitrile are added, at room temperature, 7.5 g of potassium hydrogensulphate. The mixture is stirred at a temperature of 90° C. for 3 hours. Subsequently, the mixture is cooled to room temperature and admixed with 60 ml of water and 60 ml of dichloromethane. The organic phase is removed and the aqueous phase is extracted twice with 30 ml each time of methylene chloride. The combined organic phases are concentrated to dryness. 5.95 g of 4-[[(6-chloropyridin-3-yl)methyl](2,2-difluoroethyl)amino]furan-2(5H)-one are obtained in a purity of 89% (this corresponds to 91% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273904B2
Source datasetuspto-grants-2012_09
ORD IDord-876dc1d634334d1884ebf028068e0b8a
Source noteuspto-grants-2012_09