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Ethers phenylic

Benzoylcyclohexene gives, after removal of the ether, phenyl cyclohexyl ketone, which is recrystallized from petroleum ether, mp 52° (80%). [Pg.29]

Scheme 6.17 Synthesis of poly(ether ketone) via poly(ether phenyl ketimine). Scheme 6.17 Synthesis of poly(ether ketone) via poly(ether phenyl ketimine).
Some obscurities. Each of the reactions mentioned has been identified in at least one system, but there are very many obscurities to be cleared up. For example, transfer by methyl vinyl ether, phenyl vinyl ether, vinyl acetate and some of the corresponding polymers in the polymerization of styrene by stannic chloride has been studied, but the mechanism is not at all clear [124]. [Pg.147]

A. J. Colussi, F. Zabel, and S. W. Benson, Very low-pressure pyrolysis of phenyl ediyl ether, phenyl allyl ether, and benzyl methyl-edier and endialpy of formation of phenoxy radical,/ t. J. Chem. [Pg.253]

Synonyms AI3-23460 4-BPPE jo-BPPE 4-Bromobiphenyl ether 4-Bromodiphenyl ether p Bromodiphenyl ether l-Bromo-4-phenoxybenzene 1-Bromo-p-phenoxybenzene 4-Bromophen-oxybenzene p Bromophenoxybenzene 4-Bromophenyl ether p-Bromophenyl ether p-Bromo-phenyl phenyl ether BRN 1308972 EINECS 202-952-4 NSC 5619 Phenyl-4-bromophenyl ether Phenyl-p-bromophenyl ether 4-Phenoxybromobenzene p-Phenoxybromobenzene RCRA waste number U030. [Pg.195]

For conversion of functionalized diorganozincs into tertiary amines, aromatic compounds which contain a directed metallation group, such as Af,Af-dialkylbenzamides, methoxymethyl phenyl ether, phenyl oxazolines and phenyl Af,Af-dialkylcarbamates, were ortho-lithiated, transmetallated and then aminated with 2a in good yields, but with a slower reaction rate (Scheme 19). [Pg.313]

DIPHENYL ETHER Phenyl Ether, Diphenyl Oxide, Phenoxybenzene NL, II 1 1 0... [Pg.100]

Fig. 15. Dynamic mechanical thermal behavior of poly(imide-co-phenyl ether phenyl quinoxaline)... Fig. 15. Dynamic mechanical thermal behavior of poly(imide-co-phenyl ether phenyl quinoxaline)...
Ether, phenyl 1-phenylvinyl and 2H-1-Benzopyran, 3,4-dihydro-2-methylene-)... [Pg.72]

Phenoxy-1 -phenylethene Ether, phenyl 1-phenylvinyl (8,9) (19928-57-5) 3,4-Dihydro-2-methylene-2H-1 -benzopyran 2H-1-Benzopyran, 3,4-dihydro-2-methylene- (10) (74104-13-5)... [Pg.79]

A - C11H20O C7H5NO Isobornyl methyl ether Phenyl Isocyanate 192.4 162.8 <186.0 245... [Pg.194]

A hindered secondary alcohol is oxidized with Ru04 in a polyfunctional molecule adorned by an amide, a silyl ether, phenyl rings, an ester and acetals. [Pg.226]

Phenyl acetate Ally phenyl ether Phenyl benzoate R= CII, R= Ph... [Pg.363]

Figure 3.42 a General reaction scheme for the thermal Huisgen cycloaddition b the copper-catalyzed reaction between phenyl propargyl ether (phenyl 2-propynyl ether) and benzyl azide. The catalytic reaction is performed in the presence of a reductant (sodium ascorbate) and gives just one of the product isomers in high yield. [Pg.112]

Similarly to a-naphthyl ether, one can also obtain P-naphthyl ether, phenyl ether and other aromatic ethers of pyrocatechinphosphorous acid. [Pg.429]

PHENOXY-1 -PHENYLETHENE ETHER, PHENYL 1-PHENYLVINYL (1992B-57-5), 69, 72... [Pg.156]

Ethyl glycidyl ether Phenyl glycidyl ether... [Pg.3]

Phenyl Ethers Phenyl ethers (one of the groups bonded to oxygen is a benzene ring) react with HBr or HI to give alkyl halides and phenols. Phenols do not react further to give halides because the s/r-hybridized carbon atom of the phenol cannot undergo the Sn2 (or SN1) reaction needed for conversion to the halide. [Pg.640]

Maltol Isobutyrate 2-Methoxy 3-(or 5- or 6-) Isopropyl Pyrazine 5H-5-Methyl-6,7 -dihydrocyclopenta[b]pyrazine 5-Methyl Furfural Methyl Furoate Methyl Hexanoate Methyl Isovalerate 5-Methyl 2-Phenyl 2-Hexenal Methyl Thiobutyrate Methyl Valerate P-Naphthyl Ethyl Ether Phenyl Ethyl Cinnamate Phenyl Ethyl Propionate Propyl Formate Propyl Mercaptan Salicylaldehyde 8-T etradecalactone 2-Tridecanone... [Pg.1028]

Protective group Phenyl glycidyl ether Phenyl... [Pg.121]

SYNS BENZENE, METHOXY ETHER, METHYL PHENYL FEMA No. 2097 METHOXYBENZENE METHYL PHENYL ETHER PHENYL xMETHYL ETHER... [Pg.87]

Studies primarily of effects of substituents on reactions on phenyl rings permit the assignment of nucleophilic (electron-releasing) character to various groups. These include alkyls, vinyl, hydroxyl, ether, phenyl, and... [Pg.265]

In the present context, the term electron rich alkenes refers primarily to enol ethers, enol sulfides, and A-vinylamides or A-vinylamines. Such alkenes are typically much more readily ionizable than are simple alkenes. The conversion of these substrates to the corresponding (highly electron deficient) cation radicals represents a sharp Umpolung. The Diels-Alder additions of tra j -anethole, phenyl vinyl ether, phenyl vinyl sulfide, 1,3-dioxole, and A-methylindole to 1,3-cyclohexadiene have been reported (Scheme 22) [49, 52]. [Pg.818]

If the two groups arc identical, the ether is said to be symmetrical (c.g., ethyl ether, phenyl ether), if different, unsymmetrical (e.g., methyl tert-butyl ether, anisole). [Pg.553]

Arylbismuth 671, 673 Arylboronic acid 671, 673 Arylbutenes, formation of 613 Aryl-2-cyclohexenones 653 Aryl ethers—see also AUyl aryl ethers. Diaryl ethers. Phenyl ethers, Propargyl aryl ethers formation from calixarenes 1387 Aryl haUdes, as phenol precursors 396, 397 Ai-Arylhydroxylamines, isomerization of 801-805 oxidation of 419 3-Arylindoles, synthesis of 1236 Aryl ketones, oxidation of 424, 425 Aryloxylium cations 179 Asatone, synthesis of 1178, 1179 Ash, from incineration of municipal waste, phenoUc compounds in 938 Aspersitin, synthesis of 1327, 1328 Aspirin 10, 11... [Pg.1479]

Remko, M., and I. Sekerka. 1983. MO investigations on lignin model compounds. XVI. Conformational analysis of P-aryl ether, benzyl aryl ether, phenyl coumaran, diphenyl ether and biphenyl structures. Z. Phys. Chem. (Weisbaden), 134 135-148. [Pg.346]

Mesogenic PEIs are obtained when m-aminophenol is replaced by p-ami-nophenol. A mesophase is correctly predicted in all four polymers of series 11 in Table 23. Each of the four different aromatic acids from ether diphenyl (MI score=l) to ether phenyl diphenyl (MI score=4) gives rise to a mesophase, unlike the series with pyromellitic. The Mesogenic Index approach confirms that BPTA is a much stronger mesogen than pyromellitic diimide. In fact, it predicts that if the fourth co-monomer in series 11 was an aliphatic spacer, a mesophase would still be obtained. [Pg.239]


See other pages where Ethers phenylic is mentioned: [Pg.623]    [Pg.252]    [Pg.149]    [Pg.1264]    [Pg.119]    [Pg.153]    [Pg.623]    [Pg.594]    [Pg.27]    [Pg.860]    [Pg.1151]    [Pg.302]    [Pg.9]    [Pg.623]    [Pg.703]    [Pg.12]    [Pg.36]   
See also in sourсe #XX -- [ Pg.404 ]




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0-Hydroxyphenyl phenyl ether

2,3,5,6-Tetrafluoro-4 phenyl ethers

2,3-epoxypropyl phenyl ether

2,4-Dinitrophenyl phenyl ether

2- Hydroxyethyl phenyl ethers from

2-methyl-2-propenyl phenyl ether

2.5- Dimethyl-4- phenyl benzyl ether

3- Bromoethyl phenyl ether

3-Bromo-3-phenyl methyl ether

4-Bromophenyl phenyl ether

4-Chlorophenyl phenyl ether

4-Nitrophenyl phenyl ether

4-Nitrophenyl phenyl ether preparation

A-Glyceryl phenyl ether

Allyl phenyl ether

Allyl phenyl ether Claisen rearrangement

Allyl phenyl ether preparation

Allyl phenyl ether, cyclization

Allyl phenyl ethers rearrangement

Benzyl phenyl ether

Benzyl phenyl ether, cleavage

Benzyl phenyl ethers, oxidation

Benzyl phenyl ethers, rearrangement

Bis-phenyl ethers

Butyl chloroacetate phenyl ether

Butyl phenyl ether

Chlorinated phenyl ethers

Chloromethyl phenyl ether

Choline phenyl ether

Claisen rearrangement of allyl phenyl ethers

Epoxy compounds phenyl glycidyl ether

Ether, Z-butyl phenyl

Ether, phenyl 1-phenylvinyl

Ether, tert-BUTYL phenyl

Ether-linked phenyl ring

Ethers alkyl phenyl

Ethers allyl phenyl, sigmatropic rearrangement

Ethers phenethyl phenyl, pyrolysis

Ethers phenyl, reactions with

Ethyl phenyl ether, substituted

Ethyl phenyl ether, synthesis

Ethyl phenyl ether—

Formation of phenyl ethers

Glyceryl Phenyl Ether

Hydrogenation phenyl ethers

Hydroxy-3- propyl phenyl ether

Isopropyl phenyl ether

Methyl phenyl ether—

Methyl, alcohol phenyl ether

N-Propyl phenyl ether

Of benzyl phenyl ethers

P-Bromobenzyl phenyl ether

PHENOLS AND PHENYL ETHERS

Phenethyl phenyl ether

Phenol phenyl benzyl ether

Phenol phenyl benzyl ether, effect

Phenyl 2-fluoroethyl ether

Phenyl 2-propenyl ether

Phenyl 2-pyridyl ether

Phenyl Ether

Phenyl Ether

Phenyl I butyl ether

Phenyl alkyl ethers, cleavage

Phenyl anthryl ethers (Tritylone

Phenyl ether 1- Phenylethyl alcohol

Phenyl ether 2- Phenylphenol

Phenyl ether 3-Phenylethyl acetate

Phenyl ether 3-Phenylethyl bromide

Phenyl ether 3-Phenylethyl chloride

Phenyl ether acylation

Phenyl ether bond linkages

Phenyl ether ions, decomposition

Phenyl ether-biphenyl mixture

Phenyl ether-biphenyl mixture vapor)

Phenyl ether-terminated products

Phenyl ethers 2-Phenylethylamine

Phenyl ethers compounds

Phenyl ethers reactions with 1.3-dicarbonyl

Phenyl ethers resolution

Phenyl ethers, synthesis

Phenyl ethyl thio-ether

Phenyl glycidyl ether

Phenyl glycidyl ether (PGE

Phenyl glycidyl ether epoxy

Phenyl glycidyl ether reaction

Phenyl methyl ether, cleavage

Phenyl methyl ether, protonated

Phenyl methyl ether, reaction

Phenyl n-butyl ether

Phenyl neopentyl ether

Phenyl propargyl ethers, Claisen

Phenyl propargyl ethers, Claisen rearrangement

Phenyl propyl ether ions, decomposition

Phenyl tetrazole ether

Phenyl tetrazolyl ethers

Phenyl trifluorovinyl ether

Phenyl vinyl ether

Phenyl vinyl ether, hydrolysis

Phenyl-acetic acid ether

Phenyl-indolyl ether

Phenyl/propargyl ethers

Polychlorinated phenyl ether

Polypropylene glycol alkyl phenyl ethers

Prop-2-enyl phenyl ether

Propyl phenyl ethers

Propyl phenyl ethers rearrangement

Propylene glycol phenyl ether

Rearrangement alkyl phenyl ethers

Subject alkyl phenyl ethers

Williamson ether synthesis, phenyl

Williamson ether synthesis, phenyl alkyl ethers

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