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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 332281Generated: October 27, 2026

Sodium hydride → 6-(5-Methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridine-2-carbonitrile

https://huagongshe.com/reaction/332281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant18-Crown-6HCID 28557—
Reactant6-Chloropyridine-2-carbonitrileHCID 118424—
Reactant(5-Methyl-3-phenyl-1,2-oxazol-4-yl)methanolHCID 2776149—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product6-(5-Methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridine-2-carbonitrileHCID 6844272424%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of (5-methyl-3-phenyl-isoxazol-4-yl)-methanol (189 mg, 1.0 mmol) and 6-chloropyridine-2-carbonitrile (150 mg, 1.0 mmol) in toluene (10 mL) was added sodium hydride (55% dispersion in mineral oil, 100 mg, 2.0 mmol) and the mixture heated at 50° C. for 6 h. Then 18-crown-6 (18 mg) was added and the mixture heated at 100° C. overnight. The mixture was then diluted with ethyl acetate and washed with water. The aqueous layers were extracted with ethyl acetate (10 mL) and the combined organic layers were dried over sodium sulfate. Purification by chromatography (SiO2, heptane:ethyl acetate=7:3) afforded the title compound (70 mg, 24%) as a white solid after trituration with diisopropylether. MS: m/e=292.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877783B2
Source datasetuspto-grants-2014_11
ORD IDord-28a734ed918a4e40aa2f1d2bbbbf8374
Source noteuspto-grants-2014_11