Diethyl methylenemalonate (CAS NO.: ), which is also known as , methylene-, diethyl ester, could be produced through the following synthetic routes.

A solution of 108 g. (0.5 mole) of in 100 ml. of commercial absolute alcohol is placed in an apparatus for high-pressure hydrogenation together with 10 g. of Raney nickel catalyst. The pressure in the bomb is raised to 1000–1500 lb. with hydrogen, and the temperature is adjusted to 45°. The bomb is shaken, and the reaction is allowed to proceed for 12–20 hours, during which time 0.5 mole of hydrogen is absorbed.

The apparatus is allowed to cool to room temperature, the pressure is released, and the catalyst is removed by filtration. Concentration of the filtrate under reduced pressure at room temperature yields a colorless oil.

The residual oil is transferred to a distillation flask, and the flask is carefully warmed with a small flame. After a fore-run of ethanol is collected, the variable transformer controlling the heating tape is set at a voltage to give an internal temperature in the distilling head of 80–100° before distillation. The flask is then heated to effect slow distillation at atmospheric pressure. About 10–13 g. of fore-run is collected before the temperature of the distillate vapor reaches 200°. The main fraction (68–71 g., 79–82%) is collected between 200° and 216° as a colorless oil. For most purposes, the fore-run is sufficiently pure that it can be combined with the main fraction to give an over-all yield of 78–81 g. (91–94%). Diethyl methylenemalonate polymerizes on standing to a white solid, from which the monomer can be recovered by slow distillation. The diethyl methylenemalonate should be distilled just prior to use.