2 3, p. 2 377) investigated the condensation of pyroracemic acid, CH 3 CO 000H, with various aliphatic aldehydes, and obtained from two molecules of the acid and one of the aldehyde in the presence of baryta water alkylic isophthalic acids: with acetaldehyde [1.3.51-methylisophthalic acid or uvitic acid, C 6 H 3 CH 3 (000H) 2, was obtained, with propionic aldehyde [1.3.
Grignard (Comptes Rendus, 1900 et seq.) showed that aldehydes combine with magnesium alkyl iodides (in absolute ether solution) to form addition products, which are decomposed by water with the formation of secondary alcohols, thus from acetaldehyde and magnesium methyl iodide, isopropyl alcohol is obtained.
Acetaldehyde, CH3ï¿½CHO, was first noticed by C. Scheele in 1774 and isolated and investigated by J.
(For trichloracetaldehyde see Chloral.) By the action of acetaldehyde on alcohol at Ioo° C., acetal, CH 3.
The higher aldehydes of the series resemble acetaldehyde in their general behaviour.
Scholtz (Ber., 1894, 2 7, p. 2 95 8) from piperonyl acrolein (the condensation product of piperonal and acetaldehyde) and acetic acid.
Traces of ethyl alcohol in solutions are detected and estimated by oxidation to acetaldehyde, or by conversion into iodoform by warming with iodine and potassium hydroxide.
Oxidation of ethyl alcohol gives acetaldehyde and acetic acid.
Chlorine oxidizes it to acetaldehyde, and under certain conditions chloral is formed.
It acts as an oxidizing agent, liberating iodine from potassium iodide, converting alcohol into acetaldehyde, &c.
It is readily soluble in water, melts at 193° C., and is decomposed at a higher temperature into chromium sesquioxide and oxygen; it is a very powerful oxidizing agent, acting violently on alcohol, converting it into acetaldehyde, and in glacial acetic acid solution converting naphthalene and anthracene into the corresponding quinones.
On standing with 60% sulphuric acid for some time, it is converted into the isomeric acetaldehyde-phenylhydrazone, C 6 H 5 NH N: CH CH 3 (Ber., 1896, 2 9, P. 794).
Potash fusion converts it into acetic acid; nitric acid oxidizes it to acetic and oxalic acids; chromic acid mixture to acetaldehyde and acetic acid, and potassium permanganate to a0-dioxybutyric acid.
This compound condenses in alkaline solution with compounds containing the grouping - CH 2 - CO - to form quinoline or its derivatives; thus, with acetaldehyde it forms quinoline, and with acetone, a-methyl quinoline.
In the preparation of chloroform by the action of bleaching powder on ethyl alcohol it is probable that the alcohol is ..rst oxidized to acetaldehyde, which is subsequently chlorinated and then decomposed.
The substance investigated was acetaldehyde, C 2 H 4 O, in its relation to paraldehyde, a polymeric modification.
Drewson, Ber., 1883, 16, p. 2207); by passing the vapour of allyl aniline over heated lead oxide; by the condensation of ortho-aminobenzaldehyde with acetaldehyde in the presence of aqueous.
It is also formed by the condensation of anthranilic acid with acetaldehyde (S.
Popovici, Ber., 1892, 5, 733); by the action of concentrated sulphuric acid on benzyl amino-acetaldehyde, C 6 H 5 CH 2 NH CH 2 CHO (E.
Wurtz); by boiling a-chlorpropionic acid with caustic alkalis, or with silver oxide and water; by the reduction of pyruvic acid with sodium amalgam; or from acetaldehyde by the cyanhydrin reaction (J.
In that mixture which contains 88% of paraldehyde and 12% of acetaldehyde, which the catalytic agent leaves unaffected.