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ChemicalBook CAS DataBase List Ethoxymethylenemalononitrile

Ethoxymethylenemalononitrile synthesis

4synthesis methods
Triethyl orthoformate (67.3 mg, 0.454 mol) and malononitrile (20.0 mg,0.302 mol)  were andded to acetic anhydride (77.2 gm, 0.75 moles) and the mixture was refluxed for 4-5 h at 110-140°C. The reaction was monitored by GC. After the reaction is complete, it is cooled to room temperature. Concentrated the mixture at 70°C at reduced pressure to yield crude solid product and the pure product (Ethoxymethylenemalononitrile) was obtained through purified either by vacuum distillation.
Ethoxymethylenemalononitrile
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Yield:123-06-8 98.69 %

Reaction Conditions:

with orthoformic acid triethyl ester at 120; under 2250.23 - 3750.38 Torr;Large scale;Temperature;Pressure;

Steps:

1-14

The feeding amount is 1.0 kg, and malononitrile (1.0 kg, 15.14 mol) and acetic anhydride (3.25 kg, 31.79 mol) are mixed uniformly at a room temperature, and marked as a material A; triethyl orthoformate (2.47 kg, 16.65 mol) is marked as a material B. The speed of a pump A is: 248 g/min, the speed of a pump B is: 157 g/min, the material A and the material B are respectively pumped into a continuous pipeline reactor (the volume is 50 L) by the pumps, the temperature is controlled at 120° C., the outlet back pressure of the continuous reactor is 0.3-0.5 MPa, the residence time is 100 min, the outlet sampling and gas chromatography (GC) analysis are performed, and the remaining raw material is 0.0-0.5%. A system flowing out from the continuous reactor is concentrated to 6 V under vacuum, the temperature is controlled at 20-30° C., and 4 V of n-heptane is dropwise added to the above system, after being dropwise added, the system precipitates a large amount of a solid. After being filtered, the solid is dried to obtain 1.83 kg of an ethoxymethylenemalononitrile product, the GC purity is 99.7%, and the yield is 98.69%.

References:

US2022/340517,2022,A1 Location in patent:Page/Page column 0034-0060

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