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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033017Generated: October 31, 2026

Trimethylsilyl cyanide → 2-Amino-1-(5-ethyl-2-methoxy-6-methylpyridin-3-yl)ethan-1-ol

https://huagongshe.com/reaction/1033017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl cyanideHCID 82115—
Reactant2-Methoxy-5-ethyl-6-methylnicotinaldehydeHCID 10261679—
ReactantAluminium lithium hydrideHCID 21226445—
Catalystzinc(II)iodideHCID 9883512—
SolventDiethyl EtherHCID 3283—
Product2-Amino-1-(5-ethyl-2-methoxy-6-methylpyridin-3-yl)ethan-1-olHCID 10330759—

Reaction Steps

A mixture of 2-methoxy-5-ethyl-6-methylnicotinaldehyde (1.05 g, 5.86 mmol) and trimethylsilyl cyanide (0.85 mL, 6.37 mmol) containing zinc iodide (10 mg) was stirred, under a nitrogen atmosphere, at ambient temperature for two hours. This liquid was diluted with anhydrous diethyl ether, filtered and then added dropwise to a suspension of lithium aluminum hydride (225 mg, 5.9 mmol) in diethyl ether (15 mL) under nitrogen. After two hours the reaction was quenched with saturated aqueous sodium sulfate, diluted with methylene chloride, filtered and the solvents evaporated to give a semi-solid. This residue was triturated with cold diethyl ether and the crystalline product was collected by filtration to yield 346 mg (28%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05308854
Source datasetuspto-grants-1994_05
ORD IDord-989f814f22c349e0b0631f4de664ba38
Source noteuspto-grants-1994_05