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ChemicalBook CAS DataBase List Oxobutanedioic acid
328-42-7

Oxobutanedioic acid synthesis

11synthesis methods
-

Yield:328-42-7 78%

Reaction Conditions:

with water;di[triaqua{2,6-di(phenylthiomethyl)pyridine}ruthenium(III)] tri-sulphate; pH=2.0 at 80; for 12 h;Product distribution / selectivity;

Steps:

7
[Example 7]; 0.1 mmol of water-soluble acetylene carboxylic acids whose R1 is COOH and R2 is H in Fig. 1 (a) was mixed with 2 mL of aqueous solution containing 3.1 mg (2.5 μmol) of di[triaqua {2,6-di(phenylthiomethyl)pyridine} ruthenium (III)] 3-sulphate, and the mixture was reacted at the pH 2.0 at 80°C under argon atmosphere for 12 hours. The resulting mixture was condensed to give a product. The product was analyzed by 1H NMR.

References:

Japan Science and Technology Agency EP1932824, 2008, A1 Location in patent:Page/Page column 17; 19

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