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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767542Generated: October 25, 2026

Hydrochloric Acid → 6-Methoxy-3-nitropyridine-2-acetonitrile

https://huagongshe.com/reaction/1767542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Methoxy-5-nitropyridineHCID 79525—
Reactant2-(4-Chlorophenoxy)acetonitrileHCID 306444—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product6-Methoxy-3-nitropyridine-2-acetonitrileHCID 639510—

Reaction Conditions

Temperature-12.5 °C

Reaction Steps

Under argon and in an anhydrous medium, 15 g (97.3 mmol) of 2-methoxy-5-nitropyridine and 17.9 g (107 mmol) of 4-chlorophenoxyacetonitrile are dissolved in 300 ml of anhydrous tetrahydrofuran; the solution is added by transfer to a solution of 24 g (214 mmol) of potassium tert-butylate in 220 ml of anhydrous tetrahydrofuran maintained at a temperature below −10° C. The reaction mixture is stirred for three hours at a temperature of from −10 to −15° C. An aqueous 5% hydrochloric acid solution (170 ml) is added dropwise to the reaction mixture, maintaining the temperature at −10° C. The mixture is extracted with ethyl acetate. After drying over magnesium sulphate and evaporation, the residue is purified by flash chromatography over silica gel (eluant:petroleum ether/ethyl acetate, 2:1). After washing with a petroleum ether/diethyl ether mixture (2:1), the title compound is obtained in the form of a brown product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235550B2
Source datasetuspto-grants-2007_06
ORD IDord-6803c717797c47a18d0c4bdddd647ea8
Source noteuspto-grants-2007_06