Malonic-acid sentence example

malonic-acid
  • Dibromcotinine on hydrolysis yields oxalic acid, methylamine and 0-methyl pyridyl ketone: C10H10Br2N20+3H20+0= H2C204-ECH 3 NH 2 +C 5 H 4 N 000H 3 +2HBr; whilst dibromticonine yields methylamine, malonic acid and nicotinic acid: C10H8Br2N202+ 4H20=CH 3 NH 2 +CH 2 (CO 2 H) 2 +C 5 H 4 N CO 2 H+2HBr, or if heated with zinc and caustic potash, methylamine and pyridyl-ay-dioxybutyric acid.
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  • Many esters of malonic acid have been prepared, the most important being the diethyl ester (malonic ester), CH 2 (000C 2 H 5) 2, which is obtained by dissolving monochloracetic acid in water, neutralizing the solution with potassium carbonate, and then adding potassium cyanide and warming the mixture until the reaction begins.
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  • The half nitrile of malonic acid is cyanacetic acid, CN CH 2 COOH, which, in the form of its ester, may be obtained by the action of a solution of potassium cyanide on monochloracetic acid.
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  • The true nitrile of malonic acid is methylene cyanide, CH 2 (CN) 2, which is obtained by distilling a mixture of cyanacetamide and phosphorus pentoxide.
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  • Of foremost importance are the reactions termed the malonic acid and the aceto-acetic ester syntheses; these are discussed under their own headings.
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  • Riiber (Ber., 1902, 35, p. 2411; 1904, 37, P. 22 74), by oxidizing diphenyl-2.4-cyclo-butane-bismethylene malonic acid (fron cinnamic aldehyde and malonic acid in the presence of quinoline) with potassium permanganate.
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  • The oxyderivatives of the tetrahydroand hexahydro-pyrimidines are the uracils and the ureides of malonic acid (see PuRIN).
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  • From the nitroacetic acid obtained above, malonic acid was prepared, and from this a monochlormalonic acid was obtained; we assume the chlorine atom to replace the c hydrogen atom.
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