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Nitrogen introduction

Alkalization, 19 761-762 Alkaloids, 2 71-113 in coffee, 7 253 economic aspects, 2 107-109 lysine-derived, 2 80-82 major orders bearing, 2 75 miscellaneous types, 2 106-107 nitrogen introduction into terpenoid skeleton, 2 100-105 occurrence, detection, and isolation, 2 75-77... [Pg.30]

We have also added an entirely new section dealing with semi-microanalysis. In our original Introduction (p. ix) we justified the retention of macro-methods of quantitative analysis on the grounds that they formed an excellent introduction to micromethods and also afforded a valuable training in exact manipulation generally. By now, however, the macro-estimation particularly of carbon and hydrogen and of nitrogen has disappeared entirely from most laboratories. On the other hand, the micro-... [Pg.588]

Fig. 1. Addition of the reagent with temperature control and introduction of nitrogen. Fig. 1. Reaction vessel suitable for conversions in liquid ammonia. Fig. 1. Addition of the reagent with temperature control and introduction of nitrogen. Fig. 1. Reaction vessel suitable for conversions in liquid ammonia.
The best procedures for 3-vinylation or 3-arylation of the indole ring involve palladium intermediates. Vinylations can be done by Heck reactions starting with 3-halo or 3-sulfonyloxyindoles. Under the standard conditions the active catalyst is a Pd(0) species which reacts with the indole by oxidative addition. A major con.sideration is the stability of the 3-halo or 3-sulfonyloxyindoles and usually an EW substituent is required on nitrogen. The range of alkenes which have been used successfully is quite broad and includes examples with both ER and EW substituents. Examples are given in Table 11.3. An alkene which has received special attention is methyl a-acetamidoacrylate which is useful for introduction of the tryptophan side-chain. This reaction will be discussed further in Chapter 13. [Pg.109]

Introduction of substituents on the carbocyclic ring relies primarily on electrophilic substitution and on organometallic reactions. The former reactions are not under strong regiochcmical control. The nitrogen atom can stabilize any of the C-nng o-complexes and both pyrrole and benzo ring substituents can influence the substitution pattern, so that the position of substitution tends to be dependent on the specific substitution pattern (Scheme 14.1). [Pg.135]

Highly colored, they have been used to dye cellulose acetate (552) and acrylic fibers (553). Cationic dyes prepared from 2-azothiazoles by simple alkylation on the ring nitrogen (552) have been used increasingly with the introduction of polyacrylonitrile fibers with basic sites that can be colored with such dyes (554). [Pg.105]

Summarizing, the introduction of nitrogen at the place of C-3 in thiophene does not deeply disturb the electronic environment of the sulfur atom, but it induces in the rest of the molecule some alternating modification of the electronic density (Figs. 1-3 and 1-4). The perturbations induced by the nitrogen in the tt bond order of thiophene are... [Pg.35]

Fig. 1-4. Variation of the Fig. 1-4. Variation of the <r net charges by introduction of nitrogen in piace of C-3 in thiophene.
High purity acetaldehyde is desirable for oxidation. The aldehyde is diluted with solvent to moderate oxidation and to permit safer operation. In the hquid take-off process, acetaldehyde is maintained at 30—40 wt % and when a vapor product is taken, no more than 6 wt % aldehyde is in the reactor solvent. A considerable recycle stream is returned to the oxidation reactor to increase selectivity. Recycle air, chiefly nitrogen, is added to the air introducted to the reactor at 4000—4500 times the reactor volume per hour. The customary catalyst is a mixture of three parts copper acetate to one part cobalt acetate by weight. Either salt alone is less effective than the mixture. Copper acetate may be as high as 2 wt % in the reaction solvent, but cobalt acetate ought not rise above 0.5 wt %. The reaction is carried out at 45—60°C under 100—300 kPa (15—44 psi). The reaction solvent is far above the boiling point of acetaldehyde, but the reaction is so fast that Httle escapes unoxidized. This temperature helps oxygen absorption, reduces acetaldehyde losses, and inhibits anhydride hydrolysis. [Pg.76]

Introduction of Nitrogen into a Terpenoid Skeleton. The acetate-derived fragments (35) mevalonic acid (30), which yields isopentenyl pyrophosphate (31) and its isomer, 3,3-dimethyl ally pyrophosphate (32) a dimeric C -fragment, geranyl pyrophosphate (33), which gives rise to the iridoid loganin (34) and the trimer famesyl pyrophosphate (35), which is also considered the precursor to C q steroids, have already been mentioned (see Table 3... [Pg.552]

Nearly all commercial nitrogen fertilizer is derived from synthetic ammonia. However, prior to the introduction of ammonia synthesis processes in the early 1900s dependence was entirely on other sources. These sources are stdl utilized, but their relative importance has diminished. [Pg.216]

Ammonium Sulfate. Historically ammonium sulfate was important as a fertilizer. However, since the introduction of ammonium nitrate and urea, the relative importance of ammonium sulfate worldwide has steadily decreased. In the year ended June 30, 1990, ammonium sulfate furnished only about 4% of the fertilizer nitrogen used in the United States (Fig. 3) and worldwide (Fig. 6). [Pg.221]

Manufacture is either by reaction of molten sodium with methyl alcohol or by the reaction of methyl alcohol with sodium amalgam obtained from the electrolysis of brine in a Castner mercury cell (78). Both these methods produce a solution of sodium methylate in methanol and the product is offered in two forms a 30% solution in methanol, and a soHd, which is a dry, free-flowing white powder obtained by evaporating the methanol. The direct production of dry sodium methylate has been carried out by the introduction of methanol vapors to molten sodium in a heavy duty agitating reactor. The sohd is supphed in polyethylene bags contained in airtight dmms filled in a nitrogen atmosphere. [Pg.26]


See other pages where Nitrogen introduction is mentioned: [Pg.135]    [Pg.150]    [Pg.112]    [Pg.164]    [Pg.524]    [Pg.239]    [Pg.135]    [Pg.150]    [Pg.112]    [Pg.164]    [Pg.524]    [Pg.239]    [Pg.326]    [Pg.416]    [Pg.600]    [Pg.1026]    [Pg.146]    [Pg.59]    [Pg.79]    [Pg.95]    [Pg.89]    [Pg.35]    [Pg.101]    [Pg.101]    [Pg.389]    [Pg.552]    [Pg.216]    [Pg.234]    [Pg.132]    [Pg.217]    [Pg.13]    [Pg.454]    [Pg.481]    [Pg.60]    [Pg.122]    [Pg.28]    [Pg.32]    [Pg.224]    [Pg.11]    [Pg.163]    [Pg.271]    [Pg.286]    [Pg.31]    [Pg.47]   
See also in sourсe #XX -- [ Pg.3 ]




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