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Carboxylic acid halides halides

Diaryl sulfones can be formed by treatment of aromatic compounds with aryl sulfonyl chlorides and a Friedel-Crafts catalyst. This reaction is analogous to Friedel-Crafts acylation with carboxylic acid halides (11-14). In a better procedure, the aromatic compound is treated with an aryl sulfonic acid and P2O5 in polypho-sphoric acid. Still another method uses an arylsulfonic trifluoromethanesulfonic anhydride (ArS020S02CF3) (generated in situ from ArS02Br and CF3S03Ag) without a catalyst. ... [Pg.704]

Carbon Disulfide under Sulfur Compounds Carbon Monoxide under Carbon Compounds Carbon Tetrachloride under Saturated Alkyl Halides Carbon Tetrafluoride under Saturated Alkyl Halides Carboxylic Acids Carboxylic Acids and Derivatives Carboxylic Acids with Other Functional Groups Cesium... [Pg.1265]

Halogenations with dihalotriphenylphosphoranes have been reviewed briefly by Fieser and Fieser.4 Dibromotriphenylphos-phorane appears to have been studied somewhat more than the dichloro compound, but both reagents effectively convert alcohols to alkyl halides, carboxylic acids and esters to acid halides, etc. The reaction of 1,2-epoxycyclohexane with dibromotriphenylphos-phorane under conditions similar to those described here gives a mixture of cis- and trans-1,2-dibromocyclohexanes. A reagent prepared from triphenylphosphine and carbon tetrachloride has been used for similar transformations.5... [Pg.66]

Replacement of Halogens by Fluorine in Carboxylic Acid Halides... [Pg.554]

The acylating reagents commonly used are carboxylic acid halides, RCOC1, anhydrides, (RC0)20, or the acid itself, RC02H. A strong proton or other Lewis-acid catalyst is essential. The catalyst functions to generate the acyl cation ... [Pg.1051]

Vinyl Substitutions with Carboxylic Acid Halides, Aryl Sulflnates and Arylsulfonyl Chlorides 856... [Pg.833]

Based on their chemical structure, the organic chemicals were divided into a number of categories alkanes, alkenes, amines, aromatic hydrocarbons, benzenes, carboxylic acids, halides, phenols, and sulfonic acid. Linear regression analysis has been applied using the method of least-squares fit. Each correlation required at least three datapoints, and the parameters chosen were important to ensure comparable experimental conditions. Most vital parameters in normalizing oxidation rate constants for QSAR analysis are the overall liquid volume used in the treatment system, the source of UV light, reactor type, specific data on substrate concentration, temperature, and pH of the solution during the experiment. [Pg.270]

Most compounds with triple and quadruple bonds are formed by Re, Cr, Mo, and W. The ligands in such compounds are in general relatively hard Lewis bases such as halides, carboxylic acids, and amines. Nevertheless, in some cases n-acceptor ligands such as carbonyl, phosphines and nitrile are also present. [Pg.707]

Nucleophilic substitutions reactions are those reactions in which the substitution of one nucleophile for another is involved. Alkyl halides, carboxylic acids, and carboxylic acid derivatives undergo nucleophilic substitution. However, the mechanisms involved for alkyl halides are quite different from those involved for carboxylic acids and their derivatives. The reaction of a methoxide ion with ethanoyl chloride is a nucleophilic substitution reaction (Following fig.). In it one nucleophile (the methoxide ion) substitutes another nucleophile Cl. ... [Pg.166]


See other pages where Carboxylic acid halides halides is mentioned: [Pg.153]    [Pg.177]    [Pg.244]    [Pg.983]    [Pg.181]    [Pg.103]    [Pg.194]    [Pg.370]    [Pg.226]    [Pg.227]    [Pg.229]    [Pg.231]    [Pg.233]    [Pg.235]    [Pg.237]    [Pg.239]    [Pg.241]    [Pg.243]    [Pg.245]    [Pg.247]    [Pg.249]    [Pg.251]    [Pg.253]    [Pg.255]    [Pg.69]    [Pg.1212]    [Pg.107]    [Pg.319]    [Pg.268]    [Pg.1212]    [Pg.1303]    [Pg.1338]   
See also in sourсe #XX -- [ Pg.20 , Pg.512 ]

See also in sourсe #XX -- [ Pg.21 , Pg.22 , Pg.586 , Pg.624 ]




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Acetylene and Substituted Acetylenes in Presence of Carboxylic Acids, Hydrogen Halides, Mercaptans or Amines

Acid halides

Acidic halides

Alkyl halides carboxylic acid derivatives

Alkyl halides carboxylic acid enolates

Alkyl halides, primary, oxidation carboxylic acids

Allylic halides carboxylic acids

Aryl halides carboxylic acid amide

Carbonylation carboxylic acid halides

Carboxylic Acid Derivatives Acyl Halides and Anhydrides

Carboxylic acid amid acetyl halides

Carboxylic acid amid halides

Carboxylic acid derivatives acyl halides

Carboxylic acid esters from halides

Carboxylic acid fluorides halides

Carboxylic acid halides

Carboxylic acid halides

Carboxylic acid halides aldehydes

Carboxylic acid halides palladium complexes

Carboxylic acid halides vinyl substitutions

Carboxylic acid halides vinylogous

Carboxylic acid halides: aliphatic, synthesis

Carboxylic acid halides: aliphatic, synthesis aromatic

Carboxylic acids => alkyl halides

Carboxylic acids acid halide synthesis

Carboxylic acids acid halides

Carboxylic acids acid halides

Carboxylic acids and halides

Carboxylic acids exchange with acyl halides

Carboxylic acids from acyl halides

Carboxylic acids from alkyl halides

Carboxylic acids from aryl halides

Carboxylic acids halides, degradation with

Carboxylic acids reaction with acyl halides

Carboxylic acids reaction with allylic halides

Carboxylic acids synthesis from alkyl halides

Carboxylic halides 229

Degradation (s. a. Hofmann carboxylic acids to halide

From Carboxylic Acid Hydrazides and Phosphorous Halides

From acyl halides reaction with carboxylic acids

HYDROLYSIS AND ALCOHOLYSIS OF CARBOXYLIC ACID HALIDES

Halides carboxylation

Halides carboxylic acid amides

Halides carboxylic acid esters

Halides carboxylic acids, degradation

Halides from carboxylic acids with decarboxylation

Halides, alkyl reaction with carboxylic acid salts

Halides, inorganic, with carboxylic acid

PREPARATION OF CARBOXYLIC ACIDS, ACID HALIDES, AND ANHYDRIDES

Pyridines carboxylic acid halides

Reactions with Diazonium Salts, Organic Halides, and Carboxylic Acids

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