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Tnfluoroacetic anhydride

Tnalkylindoles undergoFnedel-Crafts reactions at position 6, however, in tnfluoroacetic anhydride the a-methyl group of 1,2,3-trimethylindole is acylated through an intermediate enamine [41, 42] (equation 27) Similarly, tnfluoroacetic anhydnde acylates the double bond of the a-methylene compound shown [42] (equation 28)... [Pg.416]

Azupyrene, a nonbenzenoid 4tu tt-eleetron system, undergoes electrophilic substitution in tnfluoroacetic anhydride suggesting aromatic character, which is corroborated by spectral evidence [43] (equation 29)... [Pg.416]

Tnfluoroacetic anhydnde in a mixture with sulfuric acid is an efficient reagent for the sulfonylation of aromatic compounds [44] The reaction of benzene with this system in nitromethane at room temperature gives diphenyl sulfone in 61% yield Alkyl and alkoxy benzenes under similar conditions form the corresponding diaryl sulfones in almost quantitative yield, whereas yields of sulfones from deactivated arenes such as chlorobenzene are substantially lower [44] The same reagent (tnfluoroacetic anhydride-sulfunc acid) reacts with adamantane and its derivatives with formation of isomeric adamantanols, adamantanones, and cyclic sultones [45]... [Pg.949]

Tnfluoroacetic anhydride is an efficient dehydrating reagent [46, 47] In the presence of pyndine, it smoothly dehydrates amides and aldoximes to the correspond ing nitriles [46] and adducts of CH-acids and 1,2,3-indantnone [47] (equation 20)... [Pg.949]

Tnfluoroacetic anhydride is a good reagent for various cychzations In the presence of a catalytic amount of phosphonc acid, it is used for the macrocyclization of oi-(2-thienyl)alkanoic acids [48] (equation 21)... [Pg.949]

A useful oxidizing reagent is silver(III) tristrifluoroacetate which can be generated from silver peroxide (AgO) and a tnfluoroacetic acid-tnfluoroacetic anhydride mixture [5f] This reagent readily oxidizes alicyclic and bicyclic hydro... [Pg.950]

Tnfluoroacetic anhydride Acetic acid, trifluoro-, anhydride ... [Pg.264]

Fluoroalkyl iodides are oxidized at the iodine atom by trifluoroperoxyacetic add [779, 720] or by a mixture of tnfluoroacetic anhydride and hydrogen peroxide [77iodo]alkanes are formed in almost quantitative yields [116, 117 119]... [Pg.357]

A very common oxidizing reagent is peroxytrifluoroacetic acid, which is usually generated in situ from tnfluoroacetic acid [29, 30, 31] or tnfluoroacetic anhydride [32, 33, 34] and hydrogen peroxide Peroxytrifluoroacetic acid is one of the most efficient epoxidizing reagents [35] It can be used to prepare epoxides... [Pg.946]


See other pages where Tnfluoroacetic anhydride is mentioned: [Pg.949]    [Pg.526]    [Pg.1069]    [Pg.266]    [Pg.36]   
See also in sourсe #XX -- [ Pg.948 , Pg.949 ]

See also in sourсe #XX -- [ Pg.948 , Pg.949 ]

See also in sourсe #XX -- [ Pg.46 , Pg.98 ]

See also in sourсe #XX -- [ Pg.46 , Pg.98 ]

See also in sourсe #XX -- [ Pg.223 ]




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With tnfluoroacetic anhydride

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