HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → N-methyl-N-(3-trimethoxysilylpropyl)cyanoacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1-Propanamine, N-methyl-3-(trimethoxysilyl)- | HCID 76480 | — |
| Reactant | 2-Cyanoacetyl chloride | HCID 11051594 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-methyl-N-(3-trimethoxysilylpropyl)cyanoacetamide | HCID 86612158 | 77.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07462663B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-ebc5368094154a7d9f32eed08c71fb83 |
| Source note | uspto-grants-2008_12 |