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Carbon dioxide compounds synthesis

The key compound m the synthesis of aspirin salicylic acid is prepared from phe nol by a process discovered m the nineteenth century by the German chemist Hermann Kolbe In the Kolbe synthesis also known as the Kolbe—Schmitt reaction, sodium phen oxide IS heated with carbon dioxide under pressure and the reaction mixture is subse quently acidified to yield salicylic acid... [Pg.1006]

In addition to the processes mentioned above, there are also ongoing efforts to synthesize formamide direcdy from carbon dioxide [124-38-9J, hydrogen [1333-74-0] and ammonia [7664-41-7] (29—32). Catalysts that have been proposed are Group VIII transition-metal coordination compounds. Under moderate reaction conditions, ie, 100—180°C, 1—10 MPa (10—100 bar), turnovers of up to 1000 mole formamide per mole catalyst have been achieved. However, since expensive noble metal catalysts are needed, further work is required prior to the technical realization of an industrial process for formamide synthesis based on carbon dioxide. [Pg.509]

Hydrazine as Nucleophile. Reaction of hydrazine and carbon dioxide or carbon disulfide gives, respectively, hydrazinecarboxyhc acid [471-31-8], NH2NHCOOH, and hydrazinecarbodithioic acid [471-32-9], NH2NHCSSH, in the form of the hydrazinium salts. These compounds are useful starting materials for further synthesis. For example, if carbon disulfide reacts with hydrazine in basic medium with an alkyl haUde, an alkyl dithiocarbazate ester is obtained in a one-step reaction ... [Pg.276]

Final Purification. Oxygen containing compounds (CO, CO2, H2O) poison the ammonia synthesis catalyst and must be effectively removed or converted to inert species before entering the synthesis loop. Additionally, the presence of carbon dioxide in the synthesis gas can lead to the formation of ammonium carbamate, which can cause fouHng and stress-corrosion cracking in the compressor. Most plants use methanation to convert carbon oxides to methane. Cryogenic processes that are suitable for purification of synthesis gas have also been developed. [Pg.349]

The naturally occurring compound urea, CO(NH,), was first synthesized by Friedrich Wohler in Germany in 1828 by heating ammonium cyanate. This synthesis was a significant event because it was the first time that an organic compound had been produced from an inorganic substance. Urea may also be made by the reaction of carbon dioxide and ammonia ... [Pg.294]

Esumi, K., Sarashina, S. and Yoshimura, T. (2004) Synthesis of gold nanoparticles from an organometallic compound in supercritical carbon dioxide. Langmuir,... [Pg.58]

Anand, M., Bell, P.W., Fan, X., Enick, R.M. and Roberts, C.B. (2006) Synthesis and steric stabilization of silver nanopartides in neat carbon dioxide solvent using fluorine-free compounds. Journal of Physical Chemistry B, 110 (30), 14693-14701. [Pg.59]

Poor solubility in most common organic solvents represents an inherent problem in the synthesis and processing of many high molar mass fluoropolymers. In fact, CFCs and carbon dioxide are the best solvents for amorphous varieties of fluoropolymers. Due to the environmental problems associated with CFCs, the international community is seeking to replace them with more benign compounds such as hydrochlorofluorocarbons and hydrofluorocarbons. However, the environmental problems which will be created by the use of these replacement compounds such as the accumulation of trifluoroacetic acid in the atmosphere clouds this issue [71], Carbon dioxide presents an ideal inert solvent to effect the polymerization of these types of highly fluorinated monomers and obviates the use of solvents that are being phased out because of environmental concerns. [Pg.111]

Still another possibility in the base-catalyzed reactions of carbonyl compounds is alkylation or similar reaction at the oxygen atom. This is the predominant reaction of phenoxide ion, of course, but for enolates with less resonance stabilization it is exceptional and requires special conditions. Even phenolates react at carbon when the reagent is carbon dioxide, but this may be due merely to the instability of the alternative carbonic half ester. The association of enolate ions with a proton is evidently not very different from the association with metallic cations. Although the equilibrium mixture is about 92 % ketone, the sodium derivative of acetoacetic ester reacts with acetic acid in cold petroleum ether to give the enol. The Perkin ring closure reaction, which depends on C-alkylation, gives the alternative O-alkylation only when it is applied to the synthesis of a four membered ring ... [Pg.226]

The naphthalene-catalyzed (2.5%) lithiation of phthalan 330 (or its substituted derivatives ) in THF at room temperature allowed the preparation of the functionalized benzyllithium intermediate 331, which reacted with electrophiles at —78°C to give, after hydrolysis, the corresponding functionalized benzyl alcohols 332 (Scheme 97). When carbon dioxide was used as the electrophilic reagent, the corresponding 5-lactone was directly obtained . When carbonyl compounds were used as electrophiles, the cyclization of the resulting products 332 under acidic conditions (85% H3PO4) allows the synthesis of substituted isochromans. [Pg.702]

As we learned in Chapters 3 and 4, many inorganic compounds, not just ammonia, are derived from synthesis gas, made from methane by steam-reforming. In the top 50 this would include carbon dioxide, ammonia, nitric acid, ammonium nitrate, and urea. No further mention need be made of these important processes. We discussed MTBE in Chapter 7, Section 4, and Chapter 10, Section 9, since it is an important gasoline additive and C4 derivative. In Chapter 10, Section 6, we presented -butyraldehyde, made by the 0x0 process with propylene and synthesis gas, which is made from methane. In Chapter 11, Section 8, we discussed dimethyl terephthalate. Review these pertinent sections. That leaves only two chemicals, methanol and formaldehyde, as derivatives of methane that have not been discussed. We will take up the carbonylation of methanol to acetic acid, now the most important process for making this acid. Vinyl acetate is made from acetic... [Pg.205]

Piperidine alkaloids contain the piperidine nucleus. The structural development of this group of alkaloids in synthesis is presented in Figure 52. Here a is L-lysine and /3 is cadaverine. The basic ring of j3 is the same as in a, although the activity of PLP reduces carbon dioxide. The j3 is biogenic amine, neither a stable nor a poisonous compound... [Pg.95]

The reactions of hydrogen and oxygen to form water and carbon and oxygen to yield carbon dioxide are examples of combination reactions. A combination or synthesis reaction results when two or more substances unite to form a compound. Many other types of reactions exist. Three other common types of reactions are decomposition, single replacement, and double replacement. [Pg.55]


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See also in sourсe #XX -- [ Pg.180 , Pg.183 ]




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