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Kolbe

Kolbe reaction The pre >aration of saturated or unsaturated hydrocarbons by the electrolysis of solutions of the alkali salts of aliphatic carboxylic acids. Thus, ethanoic acid gives ethane,... [Pg.232]

A large variety of organic oxidations, reductions, and rearrangements show photocatalysis at interfaces, usually of a semiconductor. The subject has been reviewed [326,327] some specific examples are the photo-Kolbe reaction (decarboxylation of acetic acid) using Pt supported on anatase [328], the pho-... [Pg.738]

Kolb D M 1996 Reconstruction phenomena at metal-electrolyte interfaces Prog. Surf. Sc/. 51 109... [Pg.320]

Waldman D A, Kolb B U, McCarthy T J and Hsu S L 1988 Infrared study of adsorbed monolayers of poly(styrene-propylene sulphide) (PS-PPS) block copolymers Polym. Mater. Sc/. Eng. 59 326-33... [Pg.2641]

Kolb M, Botet R and Jullien R 1983 Scaling of kinetically growing clusters Phys. Rev. Lett. 51 1123-6... [Pg.2693]

Kolb D M and Franke C 1982 Surface states at the metal-electrolyte interface Appl. Phys A 49 379-87... [Pg.2756]

Franke C, Piazza G and Kolb D M 1989 The influence of halide adsorption on the electronic surface states of silver electrodes Electrochim. Acta 34 67-73... [Pg.2756]

Kolb D M, Rath D L, Wille R and Flansen W N 1983 An ESCA study on the electrochemical double layer of emersed electrodes Ber. Bunsenges. Phys. Chem. 87 1108-11 131... [Pg.2756]

Kolb D M, Kdtz R and Yamamoto K 1979 Copper monolayer formation on platinum single crystal surfaces Optical and... [Pg.2758]

Batina N, Will T and Kolb D M 1992 Study of the initial stages of copper deposition by in situ STM Faraday Discuss. 94 93-106... [Pg.2759]

Zegenhagen J, Kazimirov A, Scherb G, Kolb D M, Smilgies D-M and Feidenhans l R 1996 X-ray diffraction study of a semiconductor/electrolyte interface n-GaAs(001)/H2S04( Cu) 1996 Surf. Sc/. 352-354 346-51... [Pg.2759]

Salicylic acid. The preparation of salicylic acid by passing carbon dioxide into dry sodium phenoxide at 170-190° is the classical example of the Kolbe-Schmltt reaction. The latter is a method for introducing a carboxyl group directly into a phenol nucleus. [Pg.754]

Knoevenagel reaction Knorr pyrrole synthesis. Kolbe>Schmitt reaction Leuckart reaction Mannich reaction... [Pg.1210]

The 3.8-nonadienoate 91, obtained by dimerization-carbonylation, has been converted into several natural products. The synthesis of brevicomin is described in Chapter 3, Section 2.3. Another royal jelly acid [2-decenedioic acid (149)] was prepared by cobalt carbonyl-catalyzed carbonylation of the terminal double bond, followed by isomerization of the double bond to the conjugated position to afford 149[122], Hexadecane-2,15-dione (150) can be prepared by Pd-catalyzed oxidation of the terminal double bond, hydrogenation of the internal double bond, and coupling by Kolbe electrolysis. Aldol condensation mediated by an organoaluminum reagent gave the unsaturated cyclic ketone 151 in 65% yield. Finally, the reduction of 151 afforded muscone (152)[123]. n-Octanol is produced commercially as described beforc[32]. [Pg.445]

CARBOXYLATION OF PHENOLS ASPIRIN AND THE KOLBE-SCHMITT REACTION... [Pg.1006]

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]

Carboxylation of Phenols Aspirin and the Kolbe-Schmitt Reaction... [Pg.1007]

The Kolbe-Schmitt reaction is an equilibrium process governed by thermodynamic control The position of equilibrium favors formation of the weaker base (salicylate ion) at the expense of the stronger one (phenoxide ion) Thermodynamic control is also responsible for the pronounced bias toward ortho over para substitution Salicylate anion IS a weaker base than p hydroxybenzoate and predominates at equilibrium... [Pg.1007]

The Kolbe-Schmitt reaction has been applied to the preparation of other o hydroxy benzoic acids Alkyl derivatives of phenol behave very much like phenol itself... [Pg.1007]

Section 24 10 The Kolbe-Schmitt synthesis of salicylic acid is a vital step m the preparation of aspirin Phenols as their sodium salts undergo highly regioselective ortho carboxylation on treatment with carbon dioxide at elevated temperature and pressure... [Pg.1017]

Kolbe-Schmitt reaction (Section 24 10) The high pressure re action of the sodium salt of a phenol with carbon dioxide to give an o hydroxybenzoic acid The Kolbe-Schmitt reac tion IS used to prepare salicylic acid in the synthesis of as pinn... [Pg.1287]

Lavoisier beUeved he could distinguish acetic acid from acetous acid, the hypothetical acid of vinegar, which he thought was converted into acetic acid by oxidation. Following Lavoisier s demise, Adet proved the essential identity of acetic acid and acetous acid, the latter being the monohydrate, and in 1847, Kolbe finally prepared acetic acid from the elements. [Pg.64]

Metal Anodes" ia ECT3rd ed., VoL 15, pp. 172—183, by H. S. Holden, Diamond Shamrock Technologies, SA, and J. M. Kolb, Diamond Shamrock Corp. [Pg.125]

Hydroxy-1-Naphthalenecarboxylic Acid. 2-Hydroxy-1-naphthoic acid is manufactured by a Kolbe-type process, ie, by reaction of the thoroughly dried potassium or sodium 2-naphthalenolate with CO2 at ca 115—130°C in an autoclave at ca 300—460 kPa (3.0—4.5 atm) for 10—16 h. It decarboxylates readily, eg, in water starting at ca 50°C. [Pg.505]

Diacyl peroxides (20, R = R = alkyl or aryl) have been obtained from the oxidation of carboxyhc acid potassium salts by Kolbe electrolysis or by elemental fluorine (187). [Pg.125]

Alkylphenols undergo a carboxylation reaction known as the Kolbe Schmidt reaction. In the following example, the phenolate anion of /)-nonylphenol (15) reacts with carbon dioxide under pressure. Neutralization generates a sahcyhc acid (16) (10). [Pg.60]

T. R. Melli, W. B. Kolb, J. M. deSantos, and L. E. Scriven, "Cocurrent Downflow in Packed Beds Microscale Roots of Macroscale Plow Regimes,"... [Pg.528]


See other pages where Kolbe is mentioned: [Pg.80]    [Pg.2751]    [Pg.2756]    [Pg.30]    [Pg.378]    [Pg.546]    [Pg.111]    [Pg.213]    [Pg.239]    [Pg.521]    [Pg.423]    [Pg.501]    [Pg.505]    [Pg.404]    [Pg.187]    [Pg.294]    [Pg.111]   
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3- hydroxy-, Kolbe reaction

3- hydroxy-, Kolbe reaction oxidation

6-Alkenoic acid Kolbe electrolysis

Advances in Electrochemical Science and Engineering. Edited by Richard C. Alkire, Dieter M. Kolb

And the Kolbe reaction

Anodic Decarboxylation of Carboxylic Acids (Kolbe Electrolysis)

Anodic oxidation Kolbe coupling processes

Arene Carboxylation (Biocatalytic Kolbe-Schmitt)

Aromatic Kolbe-Schmitt synthesis

Biological Kolbe-Schmitt carboxylation

Carboxylation of Phenols Aspirin and the Kolbe-Schmitt Reaction

Carboxylic acids Kolbe electrolysis

Crossed Kolbe reaction

Decarboxylation Kolbe electrolysis

E. Kolb

Edited by Richard C. Alkire, Dieter M. Kolb, Jacek Lipkowski and Philip N. Ross

Elaidic acid Kolbe electrolysis

Electrochemistry, Kolbe electrolysis

Electrolysis, Kolbe synthesis, of 2,7dimethyl-2,7-dinitrooctane

Electrolysis, Kolbe synthesis, of 2,7dimethyl-2,7-dinitrooctane two-compartment cell for

Electroorganic synthesis Kolbe reaction

Electrooxidation Kolbe reaction

Formation of Aromatic Carboxylic Acids The Kolbe-Schmitt Synthesis

Hydrocarbons from Kolbe electrolysis

Industrial applications Kolbe—Schmitt synthesis

KOLBE Electrolysis

KOLBE SCHMIDT Salicylic acid synthesis

Kolb, Dieter

Kolb, Lawrence

Kolbe Hermann

Kolbe carboxylation

Kolbe coupling

Kolbe coupling of half esters

Kolbe coupling radical addition reactions

Kolbe cross-coupling

Kolbe dimerization

Kolbe dimerization reaction conditions

Kolbe electrolysis Subject

Kolbe electrolysis anode material

Kolbe electrolysis cathode material

Kolbe electrolysis critical potential

Kolbe electrolysis cross-coupling

Kolbe electrolysis current densities

Kolbe electrolysis electrochemical oxidation

Kolbe electrolysis ionic additives

Kolbe electrolysis mechanism

Kolbe electrolysis reaction conditions

Kolbe electrolysis solvents

Kolbe electrolysis symmetrical coupling

Kolbe electrolytic coupling

Kolbe electrolytic reaction

Kolbe electrolytic synthesis

Kolbe electrooxidation

Kolbe electrosynthesis

Kolbe electrosynthesis mechanism

Kolbe flow scheme

Kolbe nitrile synthesis

Kolbe oxidation

Kolbe product

Kolbe radicals

Kolbe radicals addition to double bonds

Kolbe reaction

Kolbe reaction cross-couplings

Kolbe reaction decarboxylation

Kolbe reaction effects

Kolbe reaction relation

Kolbe reaction stereochemistry

Kolbe reaction synthesis

Kolbe reactions radical cyclizations

Kolbe reactions reaction conditions, dimerization

Kolbe reductive coupling

Kolbe synthesis

Kolbe synthesis of nitriles

Kolbe, Adolph

Kolbe, Adolph Wilhelm

Kolbe, Adolph Wilhelm Hermann

Kolbe, Herman

Kolbe-Schmidt process

Kolbe-Schmidt reaction

Kolbe-Schmitt carbonation

Kolbe-Schmitt carboxylation

Kolbe-Schmitt carboxylation reaction

Kolbe-Schmitt method

Kolbe-Schmitt process

Kolbe-Schmitt reaction

Kolbe-Schmitt reaction Marasse modification

Kolbe-Schmitt reaction mechanism

Kolbe-Schmitt reaction,, etc

Kolbe-Schmitt synthesis

Kolbe-type synthesis

Kolbes salicylic acid synthesis

Kolbe’s reaction

Kolbe’s synthesis

Mechanisms Kolbe reaction

Methyl hydrogen sebecate Kolbe electrolysis

Non-Kolbe Reactions

Non-Kolbe electrolysis

Non-Kolbe electrolysis experimental procedure

Phenol Kolbe Schmitt reaction

Phenols Kolbe carboxylation

Phenols Kolbe reaction

Photo-Kolbe decarboxylation

Photo-Kolbe reaction

Preparation Kolbe reaction

Process Kolbe-Schmitt synthesis

Processing Kolbe-Schmitt synthesis

Reaction Parameters and Mechanistic Studies of the Kolbe-Schmitt Synthesis

Reaction with Kolbe radicals

Salicylic acid (Kolbes reaction)

Salicylic acid Kolbe synthesis

Sodium methoxide in Kolbe electrolysis

The Kolbe Reaction

Thermodynamic control Kolbe Schmitt reaction

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