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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839222Generated: October 27, 2026

Phosphorus oxychloride → 3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carbonitrile

https://huagongshe.com/reaction/839222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium AcetateHCID 517045—
Reactant3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carbaldehydeHCID 20326255—
SolventDimethylformamideHCID 6228—
Product3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carbonitrileHCID 2032615898%

Reaction Steps

Stir 5 g of 3-(5-nitro-2-furyl)-1-phenylpyrazole-4-carboxaldehyde together with 1.29 of hydroxylamine hydrochloride and 1.52 g of anhydrous sodium acetate in 15 ml of dimethylformamide for 1.5 hours at room temperature. Then add 2.85 g of phosphorus oxychloride dropwise to the resulting reaction mixture, the temperature of which rises to 40° C. Stir for 1 hour and then confirm that the reaction is complete by a thin layer chromatograph. Allow the solution to stand overnight and then pour onto 90 ml of ice water. Stir for 30 minutes at room temperature and then for 30 minutes at 40° C. Draw off the formed precipitate by vacuum filtration, wash the precipitate well with water and dry to obtain a 98% yield of 3-(5-nitro-2-furyl)-1-phenylpyrazole-4-carbonitrile [m.p. 190° to 192° C].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04093812
Source datasetuspto-grants-1978_06
ORD IDord-195df308c38b469aa2905326a54125ca
Source noteuspto-grants-1978_06