Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
  • C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
  • C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
  • C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
  • C07C45/54—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition of compounds containing doubly bound oxygen atoms, e.g. esters
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
  • C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
  • C07C45/28—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of CHx-moieties
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
  • C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
  • C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
  • C07C45/673—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by change of size of the carbon skeleton

Definitions

• the present invention relates to a process for cleaving unsaturated ketones to saturated ketones of lower molecular weight by aquathermolysis chemistry.
• Unsaturated ketones such as mesityl oxide and phorone are considered to be higher value materials with varied uses such as solvents, paint formulations, insect repellents and intermediates for organic synthesis.
• many unsaturated ketones are formed as by-products during the synthesis of simpler saturated ketones or aldehydes and, as such, constitute impurities of little commercial value which must be separated out of the reaction mixture and disposed of.
• aldol condensation of methyl ethyl ketone (MEK) formed during the zinc oxide-catalyzed oxidation of sec-butyl alcohol leads to the formation of alpha, beta unsaturated keto dimers (and higher oligomers) which may concentrate in the MEK distillation residue at levels of up to 50% by weight.
• MEK methyl ethyl ketone
• Japanese patent document JP 54/70,210 discloses the preparation of acetone from mesityl oxide by heating a product which contains mesityl oxide with aqueous alkali at temperatures equal or greater than 80°C for a period of time equal to or greater than 10 minutes.
• Netherlands patent document NL 72/6,875 teaches a similar process wherein mesityl oxide is converted to acetone by the catalytic reaction of mesityl oxide with water in the presence of cyclohexylamine and benzoic acid at 93°C for 10 minutes.
• the present invention provides a simplified process for converting unsaturated ketones having from 6 to about 24 carbon atoms into the corresponding saturated ketones comprising forming an aqueous mixture of the unsaturated ketone and at least about 50% by weight water and heating the mixture under autogeneous pressure at a temperature of from about 200° to 450°C, more preferably from about 250°C up to the critical temperature of water which is about 374°C. Heating is continued for a period of time sufficient to convert at least about 20% by weight of the unsaturated ketone, usually from about 5 up to about 120 minutes, depending on temperature, the amount of water present and the identity of the starting ketone feedstock.
• the process may be characterized as an aquathermolysis reaction wherein the reaction proceeds in water primarily through ionic routes rather than through free radical routes. Accordingly, relatively high conversion rates and good yields of saturated ketone and other reaction by-products may be obtained without the necessity of using a catalyst in the process.
• the present invention is based on the discovery that alpha, beta or beta, gamma unsaturated bonds in unsaturated ketones may be cleaved in an aqueous medium.
• the ionic reaction mechanism is facilitated largely as a consequence of the favorable changes that occur in the chemical and physical properties of water at temperatures between about 200°C up to and above the critical temperature of water which is about 374°C. These changes are manifest by water which has a higher dissociation constant, a lower density and a lower dielectric constant. These properties generally increase the solubility of the ketones in water and help facilitate ionic reaction pathways in aqueous systems, such that water serves as both a reaction medium and a source of ions.
• Unsaturated ketones which may be converted in accordance with the process of this invention include phorone and other alpha, beta unsaturated ketones having the formula 1: 2 R'
• R 3 - C (C - C -) prison C - C - R 6 « R 5 O
• R 1 and R 2 are selected from the group consisting of hydrogen and an alkyl group containing from 1 to about 4 carbon atoms
• R 3 , R 4 , R 5 , and R° are alkyl groups containing from 1 to about 4 carbon atoms and n is 0, 1 or 2.
• the process is equally applicable for the conversion of beta, gamma unsaturated ketones which are isomers of compounds having the general structure of formula 1, as well as mixtures of alpha, beta and beta, gamma unsaturated ketones.
• Inclusive of unsaturated ketones within the scope of formula 1 are mesityl oxide and other unsaturated keto oligomers which are formed as by ⁇ products during the oxidation of sec-alkyl alcohols to form the corresponding ketones. These unsaturated ketones generally contain from 6 to about 24 carbon atoms.
• acetone may be commercially produced by the oxidation of isopropyl alcohol using a suitable dehydrogenation catalyst such as zinc oxi ⁇ e.
• Methyl ethyl ketone (MEK) is produced by a similar process involving the oxidation of sec- butyl alcohol. During these oxidation steps, substantial quantities of unsaturated dimer and higher ketones are formed as a consequence of difficult-to-control Aldol condensation reactions.
• mesityl oxide may be formed as a major by-product as the result of aldol condensation of two molecules of acetone during the oxidation step.
• dimer ketones are formed as the major by ⁇ product in accordance with the following reaction scheme:
• these Aldol condensation products as well as other alpha, beta, or beta, gamma unsaturated ketones such as phorone may be readily converted to the corresponding saturated ketones by the aquathermolytic process disclosed herein wherein water serves as both the reaction medium and the catalytic source of protons and hydroxy ions.
• the amount of water used in forming the mixture with the unsaturated ketone may generally range from at least about 50% by weight up to about 97% by weight, i.e., the mixture may contain from about 1 to 30 parts by weight water per part by weight of unsaturated ketone.
• the higher the water content of the mixture within the above specified range the greater the conversion of the unsaturated ketone at any given process temperature within the 200 to 450°C range.
• the higher the process temperature within the range the less water is required to give rise to higher conversion rates of the ketone.
• the preferred water content of the mixture ranges from about 2 to about 15 parts by weight or water per part ketone, with 2 to 10 parts by weight of water being most preferred.
• the process is conducted by introducing the water and unsaturated ketone into a reaction vessel and heating the mixture under autogeneous pressure and preferably in an inert atmosphere, such as argon or nitrogen, as an aid in excluding oxygen from the system, and at a preferred temperature within the range of from about 250 to 450°C for a period of time such that a least about 20% by weight of the unsaturated ketone is cleaved at the double bond(s) and converted into other products.
• the process is conducted at a temperature not higher than the critical temperature of water which is about 374°C, but supercritical temperatures above that and up to about 450°C may also be utilized. Good results in terms of the percentage of unsaturated ketone converted and yield of saturated ketone realized are achieved with process temperatures within the range of from about 300 to 374°C.
• Acceptable conversion rates of at least about 20% by weight may be achieved by conducting the reaction over a time period of as little as 5 minutes up to 120 minutes or more. At higher temperatures and/or with higher water/ketone ratios, less time is required to achieve good conversion rates and vice versa. Most preferably the water content and reaction temperatures are such as to achieve conversion rates of at least about 50% by weight within 10 to 60 minutes, more preferably within 10 to 30 minutes.
• autogeneous pressure of the system refers to the combined vapor pressure exerted by the mixed components present in the aqueous system heated at a particular process temperature.
• the autogeneous pressure of water alone in such a system ranges from about 600 to 3200 psia over a temperature range of from about 250°C up to about 374°C.
• the autogeneous pressure of a system containing both water and the unsaturated ketone would be higher over this temperature range as a function of the ketone content and the partial pressure exerted by the ketone.
• the reaction mixture "consists of" a mixture of water and unsaturated ketone composition.
• the reaction mixture may "consist essentially of" a mixture of water and unsaturated ketone and may further include appropriate amounts of a strong or weak acid to adjust the pH of the reaction mixture in the range of from just below 7.0 down to about 2.0, or appropriate amounts of a strong or weak base to adjust the pH of the reaction mixture in the range of from just above 7.0 up to about 14.0.
• Suitable acids include phosphoric, acetic, hydrochloric or sulfuric acids; suitable bases include alkali metal hydroxides or carbonates. It has been generally found that aquathermolysis conducted in the presence of an acid or base tends to speed up the conversion process and leads to higher yields of the desired saturated ketone product because of the presence of additional protons or hydroxide ions in the system.
• the reaction mixture may also include small quantities of an ionic surfactant stable at higher temperatures to assist in enhancing the dispersibility of the unsaturated ketone in the water, particularly where higher molecular weight ketones are present.
• Preferred surfactants include anionic surfactants such as sodium lauryl sulfonate.
• SUBSTITUTE SHEET generally range from at least about 20%, preferably at least about 50% up to 100%, depending upon reaction conditions.
• the process of the present invention may be particularly adapted for use in conjunction with other chemical processes wherein unsaturated ketones are formed as a less valuable by-product as described above.
• MEK is produced commercially by the hydration of n-butylene to sec- butyl alcohol followed by oxidation of the alcohol over a ZnO catalyst to form a reaction product which comprises a mixture of MEK and unsaturated aldolized MEK dimers and heavier products.
• the residuum (bottoms) which contains the unsaturated ketones may be mixed with water and subjected to aquathermolysis in accordance with this invention to produce additional MEK.
• the process of this invention may be carried out batchwise or in the continuous mode using conventional pressure equipment.
• conventional pressure equipment include a laboratory bomb, a high pressure autoclave, a stirred tank reactor or a continuous flow-through tube, each equipped with a heating means capable of achieving and maintaining the required temperatures and pressures over the required time period.
• a laboratory-prepared unsaturated C 8 ketone was synthesized by reacting methyl ethyl ketone over AmberliteTM IRA-400 base ion exchange resin in a Soxhlet extractor to form the Aldol condensation product.
• the aldol product was then converted to the unsaturated C 8 ketone by heating it and distilling it over an acidic ion exchange catalyst (AmberlystTM 15) to provide a product having a molecular weight of 126.
• This ketone corresponds to a product of the structure of formula 1 above wherein R 1 , R 4 and R 6 are each methyl, R 3 is ethyl and n is 0.
• the product was also found to contain lesser amounts of cis and trans beta, gamma isomers where the double bond was not conjugated with the carbonyl group.
• Unconverted ketone was extracted from the reaction mixture with toluene using a known amount of pentadecane as an internal standard. This extract as well as the converted ketone (MEK) remaining in the aqueous medium were analyzed by gas chro atography which showed that 99% of the unsaturated ketone was converted with a selectivity of 100% to MEK, as shown in Table 1. Selectivity is based on the stoichiometry with two moles of MEK formed per mole of unsaturated C 8 ketone.
• Example 1 A number of additional experiments were conducted in accordance with the process of Example 1 at 315°C except that the reaction times and weight ratio of water to unsaturated C 8 ketone were varied as shown in Table 1. Also, the reaction mixture of Examples 5 and 6 included 3% by weight of acetic acid and 3% by weight of sodium hydroxide respectively. The reaction in Example 8 was conducted without the presence of water, i.e., 100% unsaturated ketone was used. Results are shown in Table 1.
• Example 1 was repeated exactly as set forth except that the ketone composition mixed with the water was a heavy ketone bottoms product obtained from the MEK distillation residue of a commercial MEK manufacturing process. This residue continued about 42% by weight of mixed unsaturated C 8 ketone isomers as well as smaller amounts of saturated C 8 ketones and C 10 , C,,, and C 12 - cyclohexene-ones.

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• Organic Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

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• 1993
  • 1993-07-05 TW TW082105401A patent/TW240219B/zh active
  • 1993-08-04 JP JP6505540A patent/JPH07509722A/ja active Pending
  • 1993-08-04 EP EP93918638A patent/EP0654022A1/de not_active Withdrawn
  • 1993-08-04 WO PCT/US1993/007331 patent/WO1994003420A1/en not_active Application Discontinuation
• 1994
  • 1994-10-06 KR KR1019940703526A patent/KR950700868A/ko not_active Application Discontinuation

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