The longchain alkylphenols are prepared by alkylation of phenol with alkenes. Realization of the oalkylation process using simple phenolic. Do phenols undergo friedel crafts alkylation reaction when. Acidcatalyzed liquidphase alkylation of phenol with. Industrially the phenol methylation is carried out by means of three types of processes.
Structure and reaction mechanism of alkylation of phenol with. Abstract o or nalkylated derivatives of aminophenols are important synthetic intermediates in organic synthesis. Mass transfer influenced the rate of alkylation of phenol and pcresol with isobutylene in a bubble column. Page 293 selective alkylation of aminophenols renchao wang and jiaxi xu state key laboratory of chemical resource engineering, and department of organic chemistry, faculty of science, beijing university of chemical technology, beijing 100 029, china email. Aqueousmediated nalkylation of amines full paper but the reaction rate is slow and it requires a longer reaction time 810 h.
Phenolic compounds can be efficiently omethylated with tetramethylammonium chloride in diglyme or polyethyleneglycol peg at temperatures of 150160 c and in the presence of either k2co3 or naoh. In opposite vapour phase alkylation is simplest and. Friedelcrafts alkylation and the application of arenes but can additionally be extended to other nucleophiles. However, under certain conditions, it is possible to form product 2 as well. Model liquid phase reactions of 1octene with phenol, catechol and guaiacol, respectively, were carried out over acid catalyst 30%cs2. As the catalyst acidity increases, 2,6 xylenol and trimethylphenol selectivity increases. One example is the addition of a methyl group to a benzene ring. This is an example of the synthesis of the reaction. Alkylation of phenol has an additional complication because of the possibility of the olefin attack to the phenolic oxygen o alkylation leading to ether formation beside the usual alkylation at the aromatic ring c alkylation. C alkylation is a process for the formation of carboncarbon bonds.
In this study, the liquidphase alkylation of phenol with linear 1octene and branched diisobutylene olefins was studied, in a batch reactor using homogeneous sulfuric acid and heterogeneous amberlyst15 acid catalysts. Study of the reaction mechanism in the alkylation of. However, 100% selectivity towards methylation was not obtained. Pdf alkylation of phenol with olefins in the presence of. However, phenol esters also undergo a fries rearrangement under friedelcrafts conditions to produce the calkylated, hydroxyarylketones. Some of the existing aqueous alkylation procedures are not successful because of the rapid hydrolysis of the alkylbenzylic halides under strongly basic conditions csoh, naoh, k 2co 3 koh, etc. In particular, monosubstituted 1,3diketones 17 and their derivatives are of great interest. This may sometimes lead to unexpected products under thermodynamic control conditions such as prolonged reaction times or at high temperatures. Efficient and selective n alkylation of amines with. Ethylation, diethyl carbonate, phenols, aryl ethyl ethers.
Dimethyl carbonate and phenols to alkyl aryl ethers synthesis. Pioneering reports dealing with the nalkylation of amines by alcohols in the presence of homogeneous catalysts were described independently by watanabe 14 and grigg 15. However, no significant improvement was observed in the yield of the monoderivative, which in some cases is the desired product. Alkylation of phenol with hexene1 in the presence of 94% sulphuric acid temperatur e 140 c, time of addition 2h, time of stirring. The main purpose of using alcl3 is to polarise the halo alkane bondalkylation. A method of alkylating a phenol is disclosed which comprises contacting a phenol having a hydrogen atom in at least one of the orthopositions relative to the hydroxyl group with an alcohol in the gaseous phase at an elevated temperature in the presence of a catalyst comprising iron oxide, silica, chromium oxide, germanium oxide and an alkali metal compound. Abstract intramolecular dearomative cyclization of phenols with. Alkylation of phenol with tertbutyl alcohol catalysed by. Alkylation definition of alkylation by the free dictionary.
The mechanism involves an exothermic reaction between olefin and the benzene sulfonic acid to form ester followed by three reaction pathways leading to direct. Oalkylation of phenol in the presence of a nucleophilic. Hence a sequence of alkylation and dealkylation steps are possible through out the reaction. From the above discussion it is clear that product selectivity in the alkylation of phenol with methanol depends mainly on the acidbase properties of the catalysts. The main purpose of using alcl3 is to polarise the halo alkane bond alkylation. The true value of altud1 is revealed in the friedelcrafts alkylation of phenol.
Alkylation of phenol with mtbe and other tertbutyl ethers. Synthesis of 2,6xylenol by alkylation of phenol with. As the title suggests im trying to alkylate a phenol, with a propargyl group. This reaction is popularly known as reimertiemann reaction. Crafts, the reaction of an alkyl halide with an aromatic compound in the presence of a lewis acid catalyst, usually alcl 3, results in the substitution of the alkyl group onto the aromatic ring. O alkylation of phenol in the presence of a nucleophilic tertiary amine. Given that the alkylation typically requires stoichiometric amounts of a base and a toxic alkyl halide the devel. Isobutylene is commercially produced mostly from the dehydration of tert butyl alcohol or from the cracking of methyl tertbutyl ether mtbe. Friedelcrafts reaction of phenol chemistry stack exchange. Alkylation of phenol with other alkenes and cresols alkylations were successfully catalysed by. Alkylation of phenol with methanol over mixed oxides of tin.
The kinetic parameters such as rate constant k, apparent activation energy ea and arrhenius frequency factor ao for the disappearance of phenol were. Apr 09, 2011 the product 1 is formed by the o alkylation of the phenolate anion, while product 2 is formed via c alkylation of the phenolate anion. Chem 1650 phenol alkylation phenol alkylation abigail. Synthesis of aryl alkyl ethers by alkylation of phenols with. In a first form, a process is provided for preparing phenol by converting acetone byproduced by the cumene process into isopropanol, and alkylating benzene with the isopropanol and optional propylene, thereby forming phenol without acetone byproduct. The reaction when carried out in the liquid phase give numerous products and their separation is difficult. Alkylation of phenol materials and process simulation center. Tandem esterification1,4additiontype friedelcrafts alkylation.
So when we add this reactant mixture to the substrate which is phenol. Isomerization of the terpene substituent as a result of rearrangements of the bicyclic myrtenol structure was observed. The alkylation of carboxylic acids with alcohols in acidic. The possibility of product 1 being formed is higher than the probability of formation of product 2. Alkylation of phenol by myrtenol in the presence of aluminum phenoxide and aluminum isopropoxide was studied in the temperature range 120160c. The reaction occurred with the formation of an array of alkylated phenols. Usually in the gas phase vapours of methanol and phenol are reacted in a flow reactor under atmospheric pressure and most frequently in the temperature range 583 0166. The regioselectivity of an alkylation with long chain olefin is really difficult to control, specifically, in the case of benzene alkylation, where there is now an increasing need to preferentially generate the more desirable 2 phenyl alkylate flch3 in equation 2 in scheme1 and to avoid the formation of nonlinear alkylbenzene.
An alkyl group can be added to a benzene molecule by an electrophile aromatic substitution reaction called the friedel. The catalyst is modeled with the benzene sulfonic acid, and the effect of this acid on olefins such as isopropene ipr and tributene tbu in a phenol solution mimics. My molecule has 2 nucleophilic centres present, the phenol and a tertiary amine, and i want o alkylation. Alkylation of phenols with isobutylene publications of the. Electrophilic substitution reactions of phenols nitration. A phenol derivative, phenolphthalein is prepared by the reaction of phenol with phthalic. Mechanistic aspects of alkylation of a general carboxylic acid. Synthesis of aryl alkyl ethers by alkylation of phenols with quaternary ammonium salts. Lewis acids are particularly suited for c alkylation. Aryl ethyl ethers prepared by ethylation using diethyl carbonate. Realization of the o alkylation process using simple phenolic. Alkylated phenols are widely used as additives in gasoline, lubricants and surfactants. Alkylation of benzene with isopropanol on mixed oxides7 and benzoylation of toluene over different sulphated zirconia and iron incorporated sulphated zi rconia systems8 have been reported. For alkylation at carbon, the electrophilicity of alkyl halides is enhanced by the presence of a lewis acid such as aluminium trichloride.
For detailed discussions on electrophilic substitution reactions of phenols, please visit byjus. The alkylation of phenol with alcohols and olefins is an important process used in industrial scale. Alkylation of phenol was carried out using methyl tertbutyl ether, mono tertbutyl ether of mono ethylene glycol, tertbutanol and. Phenol alkylation abigail sanders anna katherine edmondson introduction. Friedelcrafts alkylation reactions of phenolsnaphthols with. When phenol is treated with chloroform in the presence of sodium hydroxide, an aldehyde group is formed at the ortho position of the benzene ring.
In the case of phenol, oalkylation with ethyl methyl carbonate proceeds in the. Feb 16, 2006 the mechanism involves an exothermic reaction between olefin and the benzene sulfonic acid to form ester followed by three reaction pathways leading to direct o alkylation, oc alkylation, and pc alkylation. Ep0419045a1 method for alkylation of phenols, and catalyst. Alkylation of phenolic compounds with olefins is an important industrial reaction to increase the chemical stability of biooil. Phenol alkylation in the liquid phase is technologically unfavourable because of long reaction times, high pressure, high consumption of catalyst and troublesome regeneration. Chapter 3 friedelcrafts alkylation of phenol using ionic. Selective alkylation of phenols using solid catalysts white rose. C alkylation can also be effected by alkenes in the presence of acids. Us5015786a preparation of cumene through alkylation of an. The alkylation process combines light isoparaffins, most commonly isobutane, with c 3 c 4 olefins, to produce a mixture of higher molecular weight isoparaffins i. Liquid phase alkylation of anisole and phenol catalyzed by.
The friedelcrafts alkylation of phenol is an equilibri openi. The current work utilizes the ab initio density functional theory dft to develop a molecular level of the mechanistic understanding on the phenol alkylation in the presence of a cationexchange resin catalyst, amberlyst15. The mechanism for this reaction begins with the generation of a methyl carbocation from methylbromide. Synergism by combining various active chemistry building. Alkylation of phenol provides many industrial intermediates such as agrochemicals and polymers.
A simple method for chemoselective phenol alkylation request pdf. Vapor phase alkylation of phenol with methanol was carried out over catalysts derived from a series of hydrotalcite htlike compounds of the form miialht. In most cases the electrophile is the carbocation that is generated when the halide acts. Indeed most of the experiments show evidence of a high initial concentration of ether formation. Isobutane and c 3 c 4 olefins are produced as byproducts from fcc and other catalytic and.
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