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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228748Generated: October 30, 2026

Triethylamine → 3-Benzyloxy-6-methylpyridine-2-carbonitrile

https://huagongshe.com/reaction/228748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Nitrophthalic acid anhydrideHCID 230976—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant3-(Benzyloxy)-6-methylpicolinaldehydeHCID 22711775—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product3-Benzyloxy-6-methylpyridine-2-carbonitrileHCID 2307851254%

Reaction Steps

3-Benzyloxy-6-methyl-pyridine-2-carbaldehyde (100 mg) was dissolved in acetonitrile (5 ml) to prepare a solution. Hydroxylamine hydrochloride (72 mg) and triethylamine (0.25 ml) were added to the solution, and the mixture was stirred at room temperature for one hr. 4-Nitrophthalic anhydride was added to the reaction solution, and the mixture was stirred at 100° C. overnight. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by column chromatography using ethyl acetate-hexane to give 3-benzyloxy-6-methylpyridine-2-carbonitrile (53 mg, yield 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-bdfee52e07bc4b12b80fbb8208671e1d
Source noteuspto-grants-2009_07