ethylate's Usage Examples:

The metal also reacts with alcohol to form potassium ethylate, while hydrogen escapes, this time without inflammation: K+C 2 H 5.

Sodyl hydroxide, NaHO 2, exists in two forms: one, Na O.OH, obtained from hydrogen peroxide and sodium ethylate; the other, 0 :Na OH, from absolute alcohol and sodium peroxide at 0 °.

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°.

00 2 H 5, is obtained in the form of pearly scales when carbon dioxide is passed into an alcoholic solution of potassium ethylate, C02+KOC2H5 = KO CO.

The primary nitroparaffins combine with nitric oxide in the presence of sodium ethylate, to form nitroalkylisonitramines, R CH(NO 2) N 2 0 2 H (W.

It is prepared by oxidizing cinnamyl alcohol, or by the action of sodium ethylate on a mixture of benzaldehyde and acetaldehyde.

Darzens (Comptes Rendus, 1904, 139, p. 1214) prepares esters of disubstituted glycidic acids, by condensing the corresponding ketone with monochloracetic ester, in the presence of sodium ethylate.

With sodium ethylate in ethyl acetate solution it forms the sodium derivative of benzoyl acetone, from which benzoyl acetone, C6H5.CO.CH2.CO.CH3, can be obtained by acidification with acetic acid.

CH :CH (OH), formed by acting on formic ester with acetone in the presence of sodium ethylate, readily yields [1.3.51-triacetylbenzene, C 6 H 3 (CO CH 3) 3; oxymethylene acetic ester or formyl acetic ester or ß-oxyacrylic ester, (HO)CH :CH CO 2 C 2 H 51 formed by condensing acetic ester with formic ester, and also its dimolecular condensation product, coumalic acid, readily yields esters of [1.3.

It is a most important synthetic reagent; with sodium or sodium ethylate it forms sodio-malonic ester, which reacts readily with alkyl halides, forming alkyl malonic esters, which are again capable of forming sodium derivatives, that by further treatment with alkyl halides yield the di-alkyl malonic esters.