Alkylation pentane

Isomerization. Isomerization is a catalytic process which converts normal paraffins to isoparaffins. The feed is usually light virgin naphtha and the catalyst platinum on an alumina or zeoflte base. Octanes may be increased by over 30 numbers when normal pentane and normal hexane are isomerized. Another beneficial reaction that occurs is that any benzene in the feed is converted to cyclohexane. Although isomerization produces high quahty blendstocks, it is also used to produce feeds for alkylation and etherification processes. Normal butane, which is generally in excess in the refinery slate because of RVP concerns, can be isomerized and then converted to alkylate or to methyl tert-huty ether (MTBE) with a small increase in octane and a large decrease in RVP. 

The alkylate contains a mixture of isoparaffins, ranging from pentanes to decanes and higher, regardless of the olefins used. The dominant paraffin in the product is 2,2,4-trimethylpentane, also called isooctane. The reaction involves methide-ion transfer and carbenium-ion chain reaction, which is cataly2ed by strong acid. 

Although nitrosation of (l-dicarbonyl compounds becomes increasingly more facile upon successive replacement of the a alkyl groups with perfluoroalkyl groups because of the increased ionization of the perfluorinated enolate (equation 7), the stability of the nitrosodiketone tautomers decreases Thus, 1,1,1-trifluoro pentane-2,4-dione and 1,1,1,5,5,5-hexafluoropentane 2,4 dione mtrosate much faster than penta-2,4 dione but yield ketoximes, which decompose upon workup... 

Organolithium compounds are sometimes prepared in hydrocarbon solvents such as pentane and hexane, but nonnally diethyl ether is used. It is especially important that the solvent be anhydrous. Even trace amounts of water or alcohols react with lithium to form insoluble lithium hydroxide or lithium alkoxides that coat the surface of the metal and prevent it from reacting with the alkyl halide. Furthennore, organolithium reagents are strong bases and react rapidly with even weak proton sources to fonn hydrocarbons. We shall discuss this property of organolithium reagents in Section 14.5. 

Reductive amination of dihydropyran (which may be regarded as the dehydration product of the cyclic acetal of 5-hydroxy-pentanal) in the presence of isopropylamine and a trace of acid affords the aminoalcohol, 96. Treatment of this compound with thionyl chloride affords the haloamine, 97. Alkylation of the quinoline, 92, with this halide yields pentaquine (98). ... 

Thane et al. [46] reported that in pentane suspension, alkylaluminum compounds efficiently alkylate labile chlorines in PVC, and alternatively, PVC carbonium ions could alkylate aromatic compounds to give rise to polymers of increased stability. The values of 2-3% for labile chlorines estimated by them were considerably higher than now generally believed. 

Amyl bromide [Pentane, 1-bromo-], 82 Aniline [Benzenamine], 122 Anilines, o-alkylation of, 15 Anisole [Benzene, methoxy-], 48 Amsyl chloride [Benzene, l-(chloromethyl)-... 

These alkene isomers are separately available (4) by treatment of threo-S-trimethylsilyloctan-4-ol, prepared by reduction of the corresponding ketone with DIBAL in pentane at —120°C, with base or acid. The preparation of 5-trimethylsilyloctan-4-one itself illustrates three general procedures the addition of alkyl lithium reagents to vinylsilanes to generate a-lithiosilanes, the preparation of complex /5-hydroxysilanes, as diastereoisomeric mixtures, and the oxidation of such compounds to /8-ketosilanes... 

The relative probabilities of Reactions 24, 25, and 26 were, respectively, 1.00, 0.25, and 0.12 at a hydrogen pressure of about 1 atmosphere (9). These numbers could be derived either by analyzing the stable alkanes formed in the unimolecular decompositions (Reactions 24-26) or from the products of the hydride transfer reactions between C5Hi2 and the alkyl ions. Elimination of H2 from protonated pentane may also occur, but it is difficult (although not impossible) to establish this reaction through neutral product analysis. 

Though the syn-l,3-diol relationship is ultimately established in the reductive decyanation vide infra), the alkylation is itself highly selective. Selectivities are typically greater than 100 1 in favor of the axial nitrile. This selectivity can be rationalized by a chair-like intermediate 15 (Scheme 3) for which equatorial alkylation is highly favored on steric grounds. Approach of the electrophile from an axial trajectory leads to a syu-pentane-like interaction. 

Redistilled N, O-persilylated L-proline 438 reacts with pivaldehyde in pentane at ambient temperature to give the 0,N-acetal 439 in 78% yield in the presence of LDA this condenses, a to the carbonyl group, with N-alkyl-2-pyrrole aldehydes [48] (Scheme 5.14). 

Finally, the change in selectivity for the methane/pentane couple for the two different substrates (18% for hexane, 56% for cyclohexane) can be explained as follows in the case of cyclohexane, the Ci to C5 products are formed through the second carbon-carbon bond cleavage via the hexyl surface intermediate D whereas in the case of hexane, the initial carbon-hydrogen bond activation step can lead to any of three alkyl surface intermediates (D, E, and F) before arriving at the key metallacychc intermediates... 

Typical ion-pairing reagents are, for cations, alkyl sulphonic acids, eg pentane, hexane, heptane or octane sulphonic acid, and for anions, tetrabutylammonium or dibutylamine ammonium salts. In ion-pair chromatography the retention of solutes can be controlled in a number of ways ... 

Water (alkyl lead) Complexation of sample with diethyldithiocarbamate extraction with pentane removal of water butylation extraction with nonane GC/AAS 1.25 ng/L 90-108 Chakra borti et al. 1984... 

Evidence for the formation of alkyl and aryl radicals in some cases following loss of SO2 (Scheme 1) has been obtained. Thus, a small amount of M-pentane was formed in the decomposition of M-pentanesulphonyl azide in mineral oil ). Thermolysis of diphenyl sulphone-2-sulphonyl azide (8) in dodecane at 150 °C gave diphenyl sulphone 9 (27%) and diphenyl sulphone-2-sulphonamide 10 (9%) which arise by hydrogen abstraction by the aryl radical and sulphonyl nitrene, respectively. When this thermolysis was carried out in Freon E-4 at 150 °C, the products were diphenylene sulphone 77 (1.3%) (Pshorr-type cyclization product of the aryl radical) and 10 (1.5%) together with tars 16h Ferro-... 

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