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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374650Generated: October 30, 2026

Pyridine → N-methyl-N-(3-trimethoxysilylpropyl)cyanoacetamide

https://huagongshe.com/reaction/2374650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant1-Propanamine, N-methyl-3-(trimethoxysilyl)-HCID 76480—
Reactant2-Cyanoacetyl chlorideHCID 11051594—
SolventDiethyl EtherHCID 3283—
ProductN-methyl-N-(3-trimethoxysilylpropyl)cyanoacetamideHCID 8661215877.6%

Reaction Steps

To a 1 L reactor equipped with a thermometer, a condenser and a loading glass were added 200 mL of diethylether and 11 g of cyanoacetylchloride, followed by stirring at room temperature in the presence of nitrogen. To the reactor were slowly added 20 g of N-methylaminopropyl trimethoxysilane (0.104 mol) and 11 g of pyridine (0.14 mol) in 100 mL of diethylether by using the loading glass. The reaction mixture was stirred for 2 hours at room temperature and then the precipitated pyridine salt was eliminated. After removing the solvent and non-reactants, the reaction mixture was distilled under reduced pressure to give 21 g of N-methyl-N-(3-trimethoxysilylpropyl)cyanoacetamide (formula 3). The yield was 75%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462663B2
Source datasetuspto-grants-2008_12
ORD IDord-ebc5368094154a7d9f32eed08c71fb83
Source noteuspto-grants-2008_12