Preparation of 4-amino-2,4-dioxobutanoic acid
A process for synthesizing 4-amino-2,4-dioxobutanoic acid involves reacting diethyl oxalate with an alkoxide in ethanol to form a reaction mixture, and afterward adding ethyl cyanoacetate to the reaction mixture and allowing a reaction to proceed under conditions suitable to form a first reaction product of the formula diethyl 2-cyano-3-hydroxy-butenedioate, and then isolating the diethyl 2-cyano-3-hydroxy-butenedioate, and afterward reacting the diethyl-2-cyano-3-hydroxy-butenedioate with an aqueous hydroxide under conditions suitable to form 4-amino-2,4-dioxobutanoic acid.
1. A process for synthesizing 4-amino-2,4-dioxobutanoic acid, comprising:
reacting diethyl oxalate with an alkoxide in an alcoholic solvent to form a reaction mixture, and afterward
adding ethyl cyanoacetate to the reaction mixture and allowing a reaction to proceed under conditions suitable to form a first reaction product of the formula diethyl 2-cyano-3-hydroxy-butenedioate,
isolating said first reaction product of diethyl 2-cyano-3-hydroxy-butenedioate, and
reacting said first reaction product of diethyl 2-cyano-3-hydroxy-butenedioate with aqueous hydroxide under conditions suitable to form 4-amino-2,4-dioxobutanoic acid.
2. The process of claim 1 wherein said alkoxide is selected from the group consisting of sodium ethoxide, potassium ethoxide, lithium ethoxide, cesium ethoxide and calcium ethoxide.
3. The process of claim 1 wherein said alcoholic solvent is ethanol.
4. A process for synthesizing 4-amino-2,4-dioxobutanoic acid, comprising:
reacting diethyl oxalate with an alkoxide in a suitable solvent to form a reaction mixture, and afterward
adding ethyl cyanoacetate to the reaction mixture, and afterward
extracting the reaction mixture with a suitable organic solvent and water to form an organic layer and an aqueous layer,
then separating the aqueous layer from the organic layer,
then acidifying the aqueous layer and extracting the acidified aqueous layer with additional suitable organic solvent to form a second aqueous layer and a second organic layer,
then isolating diethyl-2-cyano-3-hydroxy-butenedioate from the second organic layer, and
then reacting the diethyl-2-cyano-3-hydroxy-butenedioate with an aqueous hydroxide under conditions suitable to form 4-amino-2,4-dioxobutanoic acid.
5. The process of claim 4 , wherein the suitable organic solvent for extracting the reaction mixture is dichloromethane.
6. The process of claim 4 wherein the first and second organic layers are combined, and the diethyl-2-cyano-3-hydroxy-butenedioate is isolated from the combined organic layers.
7. The process of claim 4 wherein said alkoxide is sodium ethoxide.
8. The process of claim 4 wherein said alkoxide is selected from the group consisting of sodium ethoxide, potassium ethoxide, lithium ethoxide, cesium ethoxide and calcium ethoxide.
9. The process of claim 4 wherein said suitable solvent is ethanol.
10. The process of claim 7 wherein said suitable solvent is ethanol.