Alkylation hydrogen fluoride

Other catalysts which may be used in the Friedel - Crafts alkylation reaction include ferric chloride, antimony pentachloride, zirconium tetrachloride, boron trifluoride, zinc chloride and hydrogen fluoride but these are generally not so effective in academic laboratories. The alkylating agents include alkyl halides, alcohols and olefines. 

The order of reactivity of the hydrogen halides parallels their acidity HI > HBr > HCl >> HF Hydrogen iodide is used infrequently however and the reaction of alco hols with hydrogen fluoride is not a useful method for the preparation of alkyl fluorides Among the various classes of alcohols tertiary alcohols are observed to be the most reactive and primary alcohols the least reactive... 

The balance of hydrogen fluoride is used ia appHcations such as stainless steel pickling inorganic fluoride production, alkylation (qv), uranium enrichment, and fluorine production. Hydrogen fluoride is used to convert uranium oxide to UF which then reacts with elemental fluorine to produce volatile UF. ... 

Isopropylnaphthalenes can be prepared readily by the catalytic alkylation of naphthalene with propjiene. 2-lsopropylnaphthalene [2027-17-0] is an important intermediate used in the manufacture of 2-naphthol (see Naphthalenederivatives). The alkylation of naphthalene with propjiene, preferably in an inert solvent at 40—100°C with an aluminum chloride, hydrogen fluoride, or boron trifluoride—phosphoric acid catalyst, gives 90—95% wt % 2-isopropylnaphthalene however, a considerable amount of polyalkylate also is produced. Preferably, the propylation of naphthalene is carried out in the vapor phase in a continuous manner, over a phosphoric acid on kieselguhr catalyst under pressure at ca 220—250°C. The alkylate, which is low in di- and polyisopropylnaphthalenes, then is isomerized by recycling over the same catalyst at 240°C or by using aluminum chloride catalyst at 80°C. After distillation, a product containing >90 wt % 2-isopropylnaphthalene is obtained (47). 

Alkyl fluorides have been prepared by reaction between elementary fluorine and the paraffins, by the addition of hydrogen fluoride to olefins, by the reaction of alkyl halides with mercurous fluoride, with mercuric fluoride, with silver fluoride, or with potassium fluoride under pressure. The procedure used is based on that of Hoffmann involving interaction at atmospheric pressure of anhydrous potassium fluoride with an alkyl halide in the presence of ethylene glycol as a solvent for the inorganic fluoride a small amount of olefin accompanies the alkyl fluoride produced and is readily removed by treatment with bromine-potassium bromide solution. Methods for the preparation of alkyl monofluorides have been reviewed. ... 

Alkylation Hazards arise from the alkylating agents, e.g. dimethyl sulphate (suspected human carcinogen), hydrogen fluoride (highly toxic irritant gas) Thermal alkylation processes require higher temperatures and pressures, with associated problems... 

Solid superacid catalysts, proposed as replacements for catalysts such as hydrogen fluoride and aluminum chloride for processes such as alkylation and acylation (Misono and Okuhara, 1993). 

Various sources of fluoride ion have been investigated, of which highly nucleophilic tetraalkylammonium fluorides ate the most effective Thuf, fluoro alkyl halides and N (fluoroalkyl)amines are efficiently synthesized by treatment of the corresponding trifluoromethanesulfonic esters with tetrabutylammonium fluoride trihydrate in aprotic solvents [5fl] (equation 34) The displacement reactions proceed quantitatively at room temperature within seconds, but tail with hydrogen fluoride-pyridine and give reasonable yields only with hydrogen fluo ride-alkylamine reagents... 

The primar> uses for hydrogen fluoride in the United States arc in the manufacture of chlorofluorocarbons, aluminum fluoride, sodium aluminum fluoride (ciyolitc). md uranium tetrafluoride, and in petroleum alkylation. 

Alkyl fluorides can be prepared by the Finkelstein reaction. The fluoride anion is a bad leaving group the reverse reaction thus does not take place easily, and the equilibrium lies far to the right. As reagents potassium fluoride, silver fluoride or gaseous hydrogen fluoride may be used. 

In order to achieve high yields, the reaction usually is conducted by application of high pressure. For laboratory use, the need for high-pressure equipment, together with the toxicity of carbon monoxide, makes that reaction less practicable. The scope of that reaction is limited to benzene, alkyl substituted and certain other electron-rich aromatic compounds. With mono-substituted benzenes, thepara-for-mylated product is formed preferentially. Super-acidic catalysts have been developed, for example generated from trifluoromethanesulfonic acid, hydrogen fluoride and boron trifluoride the application of elevated pressure is then not necessary. 

Notable examples of general synthetic procedures in Volume 47 include the synthesis of aromatic aldehydes (from dichloro-methyl methyl ether), aliphatic aldehydes (from alkyl halides and trimethylamine oxide and by oxidation of alcohols using dimethyl sulfoxide, dicyclohexylcarbodiimide, and pyridinum trifluoro-acetate the latter method is particularly useful since the conditions are so mild), carbethoxycycloalkanones (from sodium hydride, diethyl carbonate, and the cycloalkanone), m-dialkylbenzenes (from the />-isomer by isomerization with hydrogen fluoride and boron trifluoride), and the deamination of amines (by conversion to the nitrosoamide and thermolysis to the ester). Other general methods are represented by the synthesis of 1 J-difluoroolefins (from sodium chlorodifluoroacetate, triphenyl phosphine, and an aldehyde or ketone), the nitration of aromatic rings (with ni-tronium tetrafluoroborate), the reductive methylation of aromatic nitro compounds (with formaldehyde and hydrogen), the synthesis of dialkyl ketones (from carboxylic acids and iron powder), and the preparation of 1-substituted cyclopropanols (from the condensation of a 1,3-dichloro-2-propanol derivative and ethyl-... 

Alkylation and separation Refining of the hydrogen fluoride Separation of raw LAB and recycled benzene Distillation... 

As a result of alkylation LAB is obtained with a clearly changed composition in comparison with the use of chloroparaffin. With respect to the dialkyl-tetralin content, values are obtained which are comparable to LAB from the HF alkylation process (same olefin base) (Table 11). Another important difference is the 2-phenylalkane content. The isomer distribution depends on the catalyst. The reaction between straight /z-chloroparaffins or n-olefins with benzene in the presence of aluminum chloride leads to the same isomer distribution. In both cases the 2-phenylalkane content is predominant compared to the 3-, 4-, and 5-phenylalkanes. If hydrogen fluoride is used as catalyst the 2-phenylalkane... 

Catalysts like hydrogen fluoride or aluminum chloride catalyze not only the alkylation but the side reactions such as polymerization, isomerization, and disproportionation of tetrapropylene. All three side reactions are observed. In... 

Sodium LAS synthesized via aluminum chloride catalysis dissolves better than sodium LAS from the hydrogen fluoride route. The main difference is the tetralin content. Dialkyltetralinsulfonates (DATs) function as hydrotropes and this influence can be larger than that of the 2-phenylalkane content. For a homolog (equal alkyl side chains), the higher the DAT content, the lower the... 

Detal [Detergent alkylation] A process for making detergent alkylate, i.e., alkyl aromatic hydrocarbons such as linear alkyl benzenes, as intermediates for the manufacture of detergents, by reacting C10-C13 olefins with benzene in a fixed bed of an acid catalyst. Developed by UOP and CEPSA as a replacement for their Detergent Alkylate process, which uses liquid hydrogen fluoride as the catalyst. Demonstrated in a pilot plant in 1991 and first commercialized in Canada in 1996. Offered by UOP. 

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