Beckmann, Ber., 1886, 1 9, p. 9 8 9; 188 7, 20, p. 2580), yielding as final products an acid-amide or anilide, thus: RC(:N OH)R'-RC(OH) :NR' ---> As regards the constitution of the oximes, two possibilities exist, namely >C: NOH, or > C' ?, and the first of these is presumably correct, since on alkylation and subsequent hydrolysis an alkyl hydroxylamine of the type NH 2 OR is obtained, and consequently it is to be presumed that in the alkylated oxime, the alkyl group is attached to oxygen, and the oxime itself therefore contains the hydroxyl group. It is to be noted that the oximes of aromatic aldehydes and of unsymmetrical aromatic ketones frequently exist in isomeric forms. This isomerism is explained by the HantzschWerner hypothesis (Ber., 1890, 23, p. II) in which the assumption is made that the three valencies of the nitrogen atom do not lie in the same plane.
They are prepared by condensing thio-amides with a-haloid ketones or aldehydes, the thio-amide reacting as the tautomeric thio-imino acid.
CYANAMIDE, NC NH 2j the amide of normal cyanic acid, obtained by the action of ammonia on cyanogen chloride, bromide or iodide, or by the desulphurization of thio-urea with, mercuric oxide; it is generally prepared by the latter process.
Silicon nitrogen hydride, SiNH, is a white powder formed with silicon amide when ammonia gas (diluted with hydrogen) is brought into contact with the vapour of silicon chloroform at -10° C. Trianilino silicon hydride, SiH (NHC 6 H 5) 3, is obtained by the action of aniline on a benzene solution of silicon chloroform.
It crystallizes in needles which decompose at "4° C. Silicon amide, Si(NH 2) 4, is obtained as a white amorphous unstable solid by the action of dry ammonia on silicon chloride at -50° C. (E.
Wohl forms the oxime and converts it into an acetylated nitrile by means of acetic anhydride and sodium acetate; ammoniacal silver nitrate solution removes hydrocyanic acid and the resulting acetate is hydrolysed by acting with ammonia to form an amide, which is finally decomposed with sulphuric acid.
18 „ 20 „ Amide Lot 232 32 „ 23 „ EXE...,......_ 42 „ r/, 14.1/!
When heated to redness the amide is decomposed into ammonia and potassium nitride, NK 3, which is an almost black solid.
Both it and the amide decompose water readily with formation of ammonia and caustic potash.
The corresponding amide, phenyl-azo-carbonamide, C6H5N2: CONH 2, also results from the oxidation of phenylsemicarbazide (Thiele, loc. cit.), and forms reddish-yellow needles which melt at 114° C. When heated with benzaldehyde to 120° C. it yields diphenyloxytriazole, (C6H5)2CN3C(OH).
In the case of Scenedesmus acutus it is said that the alga is unable to take up nitrogen in the form of a nitrate or ammoniacal salt, and requires some such substance as an amide or a peptone.
UREA, or Carbamide, Co(NH2)2, the amide of carbonic acid, discovered in 1773 by H.
Or by heating the amide salts of the alkyl dithio-carbaminic acids, viz., NR CS S(NH 3 R).
Barium amide, Ba(NH 2) 2, is obtained from potassammonium and barium bromide.
It is an optically active liquid which boils at 168-169° C. Homologues of menthone may be obtained from the ketone by successive treatment with sodium amide and alkyl halides (A.
One was obtained in the form of its amide by the reduction of benzamide in alkaline solution with sodium amalgam (A.
Cyclo-heptene, C 7 H 121 is obtained by the action of alcoholic potash on suberyl iodide; and from cyclo-heptane carboxylic acid, the amide of which by the action of sodium hypobromite is converted into cyclo-heptanamine, which, in its turn, is destructively methylated (R.
Amino-cyclo-heptane (suberylamine) is obtained by the reduction of suberone oxime or by the action of sodium hypobromite on the amide of cycloheptane carboxylic acid.
By the action of bromine and alcoholic potash on the amides,, they are converted into amines containing one carbon atom less than the original amide, a reaction which possesses great.