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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2365760Generated: October 25, 2026

Hydrochloric Acid → HCID 178509386, compound

https://huagongshe.com/reaction/2365760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethyl SulfateHCID 6497—
ReactantMalononitrileHCID 8010—
Reactant4-Nitrobenzoyl chlorideHCID 8502—
ReactantHydrazineHCID 9321—
ReactantSodium hydrideHCID 24758—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 178509386HCID 17850938628.4%

Reaction Steps

A 1000 mL round bottom flask was pre-cooled in an ice-water bath, to which a solution of malononitrile (10.2 g, 0.154 mol) was mixed into a suspension of sodium hydride (6.72 g, 0.28 mol) in THF (100 mL). To this mixture, 4-nitrobenzoyl chloride (26 g, 0.14 mol; Sigma-Aldrich) was added slowly. After 20 minutes, the reaction was removed from the ice-water bath and left stirring for 2 hours. Dimethyl sulfate (16 mL, 0.168 mol) was then added with a syringe. The reaction vessel was placed into an oil bath at 90° C. and almost immediately afterwards a yellow solid began to form. The reaction was left at 90° C. for 2 hours. The reaction mixture was removed from the oil bath and allowed to cool to room temperature. Afterwards, hydrazine (7.5 mL, 0.154 mol) was added, and the reaction was left stirring for 60 minutes. 200 mL of brine and 100 mL of 2N HCl were added and separated from the organic layer. The aqueous phase was extracted two additional times with CH2Cl2. The organic phases were combined and concentrated in vacuo to yield a bright yellow solid. The solid was suspended in 100 mL EtOH, refluxed for 30 minutes, and the insoluble solid was collected by filtration, washed with room temperature EtOH, and dried to yield 5-amino-3-(4-nitrophenyl)-1H-pyrazole-4-carbonitrile (9.1 g, 28% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697709B2
Source datasetuspto-grants-2014_04
ORD IDord-50e453b283484924a8ef676a49f4a802
Source noteuspto-grants-2014_04