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Chloride, methylation

The rate of the reaction decreases with increasing number of substituents in the acetylenic halide, and it is higher with acetylenic bromides than with the corresponding chlorides. Methyl magnesium iodide gives equal amounts of 1,1- and 1,3--substitution products, whereas tert.-butylmagnesium bromide does not react. However, for some tert.-butyl substituted allenes there exists an attractive com-... [Pg.152]

Copolymerization can be carried out with styrene, acetonitrile, vinyl chloride, methyl acrylate, vinylpyridines, 2-vinylfurans, and so forth. The addition of 2-substituted thiazoles to different dienes or mixtures of dienes with other vinyl compounds often increases the rate of polymeriza tion and improves the tensile strength and the rate of cure of the final polymers. This allows vulcanization at lower temperature, or with reduced amounts of accelerators and vulcanizing agents. [Pg.398]

Chlorine atom Methane Hydrogen chloride Methyl radical... [Pg.172]

CeUulose triacetate is insoluble in acetone, and other solvent systems are used for dry extmsion, such as chlorinated hydrocarbons (eg, methylene chloride), methyl acetate, acetic acid, dimethylformamide, and dimethyl sulfoxide. Methylene chloride containing 5—15% methanol or ethanol is most often employed. Concerns with the oral toxicity of methylene chloride have led to the recent termination of the only triacetate fiber preparation faciHty in the United States, although manufacture stiH exists elsewhere in the world (49). [Pg.296]

Cd/Cd compounds carbon tetrachloride chloroform Cr/Cr compounds CN-compounds /HCN Pb/Pb compounds Hg/Hg compounds methylene chloride methyl ethyl ketone methyl isobutyl ketone Ni/Ni compounds tetrachloroethylene toluene... [Pg.153]

Majima et al. prepared ethyl y-(3-indolyl)-y-oxobut3rrate (250) in a similar manner by the condensation of the indole Grignard reagent with -ethoxycarboiiylpropionyl chloride.Methyl y-(3-indolyl)-y-oxobutyrate (251) has been obtained by the action of mcthoxycarbonylpropionyl chloride on indole magnesium iodide in ether. Ballantine et al. prepared methyl y-(5-methoxy-3-... [Pg.77]

Xanthene-9-carboxylic acid 3-Diisopropylaminoethyl chloride Methyl bromide... [Pg.1311]

Microwave studies of equilibrium orientations of methyl groups show that the forces act like repulsions, i.e., the hydrogens are staggered with respect to the atoms at the other end, at least in ethyl chloride, methyl silane, methyl fluorosilane, and methyl germane. Where there are only two attached atoms at one end, one connected by a single, the other by a double bond, as in acetaldehyde, propylene, acetyl fluoride and chloride, one of the methyl hydrogens is opposite the double bond, i.e., eclipsed. [Pg.383]

Methanol, ethanol, acetone, methylene chloride, methyl acetate, THF, methyl cellosolve, ethyl cellosolve, butyl cellosolve, n-xylene, p-xylene, and o-xylene... [Pg.117]

Benzoxepin, 55, 89 Benzoyl chloride, 55, 123 Benzyl chloride [Methyl chloride, phenyl-], 55,94... [Pg.139]

Isobutylene, methyl chloride, methyl bromide, ethyl chloride (Linde Div. Union Carbide Corp.) were obtained in high purity and were further purified by passing through a column containing barium oxide and molecular sieves. [Pg.89]

CH3CI 74-87-3) see Atropine methonitrate Clobazam Dimethyltubocurarinium chloride Methylmethionine sulfonium chloride Naproxen Suxamethonium chloride methyl chloroacetate... [Pg.2413]

Methylene chloride Methyl ethyl ketone (MEK), see 2-Butanone 13.4... [Pg.233]

Besides benzyl chloride, methyl- and/or chlorine-substituted benzyl chlorides, phenethyl chloride, etc. are also successfully employed to give 2 -diaralkylaminofluorans in excellent yield. However, aryl halides such as chlorobenzene and bromobenzene hardly enable the reaction, though aryl iodides such as iodobenzene give 2 -diarylaminofluorans in low yield. [Pg.191]

COMPOUND NAME CHLORODIFLUOROMETHANE DICHLOROFLUOROMETHANE CHLOROFORM HYDROGEN CYANIDE DIBROMOMETHANE DICHLOROMETHANE FORMALDEHYDE FORMIC ACID METHYL BROMIDE METHYL CHLORIDE METHYL FLUORIDE METHYL IODIDE NITROMETHANE METHANE METHANOL METHYL MERCAPTAN METHYL AMINE METHYL HYDRAZINE METHYL SILANE... [Pg.940]

Dichloroethylene Methylene chloride Methyl chloride Trichloroethylene... [Pg.321]

Pentamethyl benzene.—Fraction V, and xylene which is methylated beyond the tetramethyl benzene stage, may be worked up for pentamethyl benzene. If xylene is to be methylated to obtain pentamethyl benzene, one more mole of methyl chloride should be used, and the mixture of xylene and anhydrous aluminium chloride methylated for one hundred and ten hours instead of the one hundred used for durene. Otherwise the procedure is exactly the same as for durene. The reaction mixture is decomposed and fractionated in the usual way, and the material boiling above 205° (fraction V) is separated into three frac-... [Pg.18]

Methyl acetate Methyl acrylate Methyl r-butyrate Methyl w-butyrate Methyl chloride Methyl ethyl ketone Methyl formae Methyl iodide Methyl propionate Mehyl propyl ketone Methyl sulfide Naphthalene Nitric acid Nitric acid, 60% Nitrobenzene Nitrogen dioxide Nitrotoluene Octane Octyl alcohol Pentachloroethane Pentane Phenol... [Pg.485]

Lovelock and co-workers [228,229] determined methyl fluoride, methyl chloride, methyl bromide, methyl iodide, and carbon tetrachloride in the Atlantic Ocean. This shows a global distribution of these compounds. Murray and Riley [230,231] confirmed the presence of carbon tetrachloride, and also found low concentrations of chloroform and tri- and tetrachloroethylene in Atlantic surface waters. [Pg.406]

Many other glycosides have been subjected to selective chlorination with sulfuryl chloride. Methyl /3-L-arabinopyranoside afforded methyl 4-chloro-4-deoxy-a-D-xylopyranoside 2,3-di(chlorosulfate) in 29% yield, whereas the a-L anomer gave357 methyl 3,4-dichloro-3,4-dideoxy-/3-i)-ribopyranoside 2-(chlorosulfate) (30%). Methyl /3-d-ribopyranoside was converted into methyl 3,4-dichloro-3,4-dideoxy-a-L-arabinopyranoside through the action of pyridine hydrochloride on its 2,3,4-tri(chlorosulfate).358 Methyl a-D-lyxopyranoside gave only the 2,3,4-tri(chlorosulfate),353 as would be expected from the disposition of its hydroxyl groups, similar to that in the rhamno- and manno-pyranosides. Methyl a-D-altropyranoside was transformed into the 6-chloro-6-deoxy 2,3,4-tri(chlorosulfate) derivative in 80% yield.353... [Pg.75]

A process plant inventories the following chemicals vinyl chloride, methyl ethyl ketone, ethylene oxide, styrene, and cyclohexane. Determine the hazards associated with these chemicals. What additional information might you request to perform an appropriate assessment of the risk associated with these chemicals ... [Pg.104]

Figure 2. Degradation of a Vinylidene Chloride/Methyl Acrylate (Five Mole percent)/ 4-Vinylpyridine (0.1 Mole Percent) Terpolymer at 170 °C. Figure 2. Degradation of a Vinylidene Chloride/Methyl Acrylate (Five Mole percent)/ 4-Vinylpyridine (0.1 Mole Percent) Terpolymer at 170 °C.

See other pages where Chloride, methylation is mentioned: [Pg.420]    [Pg.303]    [Pg.1055]    [Pg.323]    [Pg.447]    [Pg.347]    [Pg.506]    [Pg.127]    [Pg.793]    [Pg.196]    [Pg.205]    [Pg.250]    [Pg.458]    [Pg.96]    [Pg.302]    [Pg.1270]    [Pg.380]    [Pg.271]    [Pg.107]    [Pg.132]    [Pg.227]    [Pg.587]    [Pg.74]    [Pg.75]    [Pg.276]   
See also in sourсe #XX -- [ Pg.11 , Pg.374 ]




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