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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349538Generated: October 30, 2026

Sodium hydride → 3-(1-Methyl-5-triphenylmethylaminopyrazol-4-yl)acrylonitrile

https://huagongshe.com/reaction/349538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantDiethyl (cyanomethyl)phosphonateHCID 75676—
Reactant1-Methyl-5-triphenylmethylaminopyrazole-4-carbaldehydeHCID 17961960—
SolventTetrahydrofuranHCID 8028—
Product3-(1-Methyl-5-triphenylmethylaminopyrazol-4-yl)acrylonitrileHCID 6933174560.9%

Reaction Steps

To a suspension of sodium hydride (55% dispersion in mineral oil, 26.2 g, 600 mmol) in tetrahydrofuran (1000 ml) was added diethyl(cyanomethyl)phosphonate (106.3 g, 600 mmol) under ice-cooling. The mixture was stirred under ice-cooling for 20 minutes. To the mixture was added 1-methyl-5-triphenylmethylaminopyrazole-4-carbaldehyde (197 g, 530 mmol), and the mixture was stirred for 2 hours. The reaction mixture was poured into ice-cold water. The mixture was extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The residue was triturated with diethyl ether to give 3-(1-methyl-5-triphenylmethylaminopyrazol-4-yl)acrylonitrile (E, Z mixture, 126 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179801B2
Source datasetuspto-grants-2007_02
ORD IDord-efdb7497533745a4a77875ee3583e194
Source noteuspto-grants-2007_02