6-trichlor-5-methylpyrimidine by the action of sodium methylate.

By the direct action of hydroxylamine on a methyl alcohol solution of mesityl oxide in the presence of sodium methylate a hydr oxylamino - ketone, diacetone hydroxylamine, (CH 3) 2 C(Nhoh) CH20OCH3,is formed.

Carbon monoxide takes part in the syntheses of sodium formate from sodium hydrate, or soda lime (at 200 0 -2 20 0), and of sodium acetate and propionate from sodium methylate and sodium ethylate at 160 0 -200°.

Meyer, Ber., 1876, 9, P. 543), C3H7NH 2 +HNO 2 =N 2 +2H 2 O+C 3 H 6; by the electrolysis of the alkali salts of saturated dicarboxylic acids; by the decomposition of 0-haloid fatty acids with sodium carbonate, CH 3 CHBr CH(CH 3) CO 2 H =CO 2 -1-HBr+CH 3 CH :CH CH 3; by distilling the barium salts of acids Cn,H 2, ,,- 2 0 2 with sodium methylate in vacuo (I.

Well-dried hydroxylamine hydrochloride is dissolved in methyl alcohol and mixed with sodium methylate; a solution of methyldichloramine in absolute ether is then added and an ethereal solution of diazomethane distils over.

They form unstable addition products with sodium ethylate or methylate.

It crystallizes in prisms which melt at 121° C. It yields addition compounds with aniline and naphthalene, and combines directly with potassium methylate, sodio-malonic ester and hydrocyanic ester.

Ramsay, Ber., 1877, 10, p. 736); by heating pyrrol with sodium methylate and methylene iodide to 200° C. (M.

Lobry de Bruyn from the hydrochloride, by dissolving it in absolute methyl alcohol and then adding sodium methylate.

methylate DNA.

6-trichlor-5-methylpyrimidine by the action of sodium methylate.

By the direct action of hydroxylamine on a methyl alcohol solution of mesityl oxide in the presence of sodium methylate a hydr oxylamino - ketone, diacetone hydroxylamine, (CH 3) 2 C(Nhoh) CH20OCH3,is formed.

Carbon monoxide takes part in the syntheses of sodium formate from sodium hydrate, or soda lime (at 200 0 -2 20 0), and of sodium acetate and propionate from sodium methylate and sodium ethylate at 160 0 -200°.

Meyer, Ber., 1876, 9, P. 543), C3H7NH 2 +HNO 2 =N 2 +2H 2 O+C 3 H 6; by the electrolysis of the alkali salts of saturated dicarboxylic acids; by the decomposition of 0-haloid fatty acids with sodium carbonate, CH 3 CHBr CH(CH 3) CO 2 H =CO 2 -1-HBr+CH 3 CH :CH CH 3; by distilling the barium salts of acids Cn,H 2, ,,- 2 0 2 with sodium methylate in vacuo (I.

Well-dried hydroxylamine hydrochloride is dissolved in methyl alcohol and mixed with sodium methylate; a solution of methyldichloramine in absolute ether is then added and an ethereal solution of diazomethane distils over.

They form unstable addition products with sodium ethylate or methylate.

C 2 H 5, is prepared from methyl iodide and sodium ethylate, or from ethyl iodide and sodium methylate (A.

It crystallizes in prisms which melt at 121° C. It yields addition compounds with aniline and naphthalene, and combines directly with potassium methylate, sodio-malonic ester and hydrocyanic ester.

Ramsay, Ber., 1877, 10, p. 736); by heating pyrrol with sodium methylate and methylene iodide to 200° C. (M.

Lobry de Bruyn from the hydrochloride, by dissolving it in absolute methyl alcohol and then adding sodium methylate.