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Esterification alkylative

Chemical Properties. MSA combines high acid strength with low molecular weight. Its pK (laser Raman spectroscopy) is —1.9, about twice the acid strength of HCl and half the strength of sulfuric acid. MSA finds use as catalyst for esterification, alkylation, and in the polymerisation and curing of coatings (402,404,405). The anhydrous acid is also usefijl as a solvent. [Pg.154]

In a similar scheme, acylation of 2-methoxynaphthalene gives ketone, 15. This is then converted to the acetic acid by the Wilgerodt reaction. Esterification, alkylation of the carbanion (sodium hydride methyl iodide), and finally saponification affords naproxen (17). The intense current effort on nonsteroid antiinflammatory agents and acrylacetic acids in particular make... [Pg.86]

Liquid-liquid reactions occur between two or more liquid phases whereby a system consisting of an organic and an aqueous phase is applied most frequently. Usually reaction takes place in one phase only. Phase-transfer catalysts are sometimes used to make transfer of a reactant to the reacting phase easier. Among typical liquid-liquid reactions utilized in fine chemicals manufacture are nitrations with mixtures of nitric and sulphuric acid, conventional hydroxylations performed with hydrogen peroxide, esterifications, alkylations, brominations, and iodinations. [Pg.261]

ESTERIFICATION Alkyl chloroformates. 4-(N,N-Diemethylaminc )pyridinium chloro-sulfite chloride. 1, r-Di(methylcyclo-pentadienyl)tin. Ethyl acetoacetate. N,N,N, N -Tetramethylchloroformami-dinium chloride. [Pg.661]

Esterification/ alkylation, deNOx reaction, hydrogenation, and Zeolite molecular sieve membrane It is found that zeolite membranes, disk, and coating show high performance or potential as catalysts compared with conventional catalysts [160]... [Pg.131]

Use Catalyst in esterification, alkylation, olefin polymerization, peroxidation reactions. [Pg.810]

Comparison data were presented, that demonstrate the use of the polysiloxane material as an advantageous substitute for organic cation exchange resins, sulfuric acid, p-toluene sulfonic acid and acidic zeolites. It is demonstrated, that materials like 1 and 2 are cost-efficient and reliable catalysts in esterification, alkylation, and condensation, whereas use of the bifunctional catalyst 3 gives excellent conversions in hydrogenolysis reactions in general. [Pg.74]

Isobutylene Oxidnlion - Esterification Alkylation - Methyl methacrylate - p-l-bulylphenol -v Organic glass - Resins... [Pg.196]

Soybean oil may be hydrolyzed into glycerol and fatty acids, or soybean oil soap-stocks (foots) may be acidified to produce fatty acids. Crude soybean fatty acids are used to make adhesive tape, shaving compounds, textile water repellents, carbon paper, and typewriter ribbons. Consumption of fatty acids in the United States, Western Europe, and Japan was 2.3 MMT (2.5 million t) in 2001. These soybean fatty acids can be separated into various fractions by distillation, and are used in candles, crayons, cosmetics, polishes, buffing compounds, and mold lubricants. These fatty acids can be converted to FAME by esterification, alkyl epoxy esters by epoxidation, fatty alcohols by hydrogenation (Kreutzer, 1983 Voeste Buchold, 1983), and dimer and trimer acids by conjugation or amines and amides as shown in Fig. 17.7 (Maag, 1983). [Pg.595]

Acetyl-6-methoxy-naphthalene may be prepared by the acylation of 6-methoxynaphthalene. The resulting product is then subjected to a series of reactions, namely Wilgerodt-Kindler reaction, esterification, alkylation and hydrolysis ultimately yields /)Z-Naproxen. Resolution of the resulting racemic mixture is caused through precipitation of the more potent /)-enantiomer as the cinchonidine salt. [Pg.533]

Esterification/alkylation, deNOx reaction, hydrogenation, and dehydrogenation studied... [Pg.207]

Uses Chemical synthesis intermediates esterification/alkylation/ hydroisomerization/acylation catalyst reactant polymerization of epoxies, styrenes, and THF petroleum refining explosives dyes paints electrolytes formation of biaryls foods (catalyst in prod, of cocoa butter substitute from palm oiO catalyst for pharmaceuticals Reguiatoty FDA 21CFR 173.395... [Pg.1397]

Uses Chemical synthesis intermediates esterification/alkylation/hydroisomerization/ac... [Pg.4529]


See other pages where Esterification alkylative is mentioned: [Pg.94]    [Pg.361]    [Pg.260]    [Pg.6]    [Pg.424]    [Pg.51]    [Pg.217]    [Pg.370]    [Pg.371]    [Pg.51]    [Pg.260]    [Pg.51]    [Pg.80]    [Pg.1190]    [Pg.90]    [Pg.914]    [Pg.2550]    [Pg.560]    [Pg.112]   
See also in sourсe #XX -- [ Pg.6 , Pg.335 ]

See also in sourсe #XX -- [ Pg.6 , Pg.335 ]




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Alkylation (esterification)

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