Organic compounds -- part of the class 532-570 series – Organic compounds – Oxygen containing
Reexamination Certificate
2001-09-05
2002-12-24
Lambkin, Deborah O. (Department: 1626)
Organic compounds -- part of the class 532-570 series
Organic compounds
Oxygen containing
C568S648000
Reexamination Certificate
active
06498278
ABSTRACT:
FIELD OF THE INVENTION
The present invention relates generally to a process for the preparation of hydroxyalkyl ether compounds. More particularly, the present invention is concerned with the preparation of &ggr;-hydroxy ether compounds by reacting species having active hydrogen atoms with organic carbonates containing six-membered rings.
BACKGROUND OF THE INVENTION
Methods exist for the alkoxylation of organic carbonates such as ethylene carbonate and propylene carbonate by reacting them with certain organic compounds including phenols and alcohols to produce &bgr;-hydroxy ethers.
&bgr;-Hydroxy ethers are currently widely used in a number of different applications. &ggr;-Hydroxy ethers may be used in place of &bgr;-hydroxy ethers as functional fluids or as spacers in the synthesis of urethane and/or ester containing polymer formulations.
The methods used to prepare &bgr;-hydroxy ethers typically do not provide for satisfactory synthesis of &ggr;-hydroxy ethers, giving unacceptably low yields. Therefore, there is a need for a process by which &ggr;-hydroxy ethers may be readily prepared.
SUMMARY OF THE INVENTION
The present invention provides a method for the preparation of &ggr;-hydroxy ethers from cyclic organic carbonates and active-hydrogen-containing compounds.
The method of the present invention includes the steps of contacting an active-hydrogen-containing compound, a cyclic organic carbonate compound containing a six-membered ring, and a catalyst.
The reaction is run at a suitable temperature, and the &ggr;-hydroxy may be isolated as a mixture that can be purified or used directly as produced in the reaction.
DETAILED DESCRIPTION OF THE INVENTION
The present invention is a process that includes providing a hydroxylated or thiolated aromatic compound (containing an “active-hydrogen species”), a cyclic organic carbonate containing a six-membered ring, and a catalyst; and reacting the active-hydrogen species and the cyclic organic carbonate in the presence of the catalyst to form an alkoxylated compound as depicted below
where R
1
through R
6
are each independently hydrogen or a linear or branched alkyl group, Ar is an aryl group, and X is oxygen, sulfur, or nitrogen.
The active-hydrogen species that may be employed are numerous and known in the art. The term “active-hydrogen species” in this application means any compound with a sufficiently acidic hydrogen atom to under go the reaction depicted above. These include, but are not limited to, both mono- and polyhydric phenols and thiophenols, phenolic resins, aniline, cyanuric acid.
Examples of monohydric phenols which may be employed generally include phenol, &bgr;-naphthol; p,p′-sec-butylidenediphenol; o-chlorophenol; o-cresol; p-propyl phenol; p-bis(o-cresol); phenyl phenol; nonyl phenol; mono-; di-; and tri-alkyl phenols; C
1
to C
18
substituted phenols, such as nonylphenol; polyaralkylphenols; halophenols; arylphenols; naphthols; and hydroxyquinoline.
Examples of some useful di- and polyhydric hydroxyl compounds include Bisphenol A; cyanuric acid; catechol; resorcinol; hydroquinone; 4,4′-biphenol; 4,4′-isopropylidenebis(o-cresol); 4,4′-isopropylidenebis(2-phenylphenol); alkylidenediphenols such as bisphenol A, pyrogallol, and phloroglucinol; naphthalenediols; phenol/formaldehyde resins; resorcinol/formaldehyde resins; and phenol/resorcinol/formaldehyde resins.
Exemplary thiophenols include thiophenol; o-thiocresol; m-thiocresol; p-thiocresol; 4,4′-thiodiphenol; and 4,4′-thiobisbenzenethiol. Alkaline salts of phenols may also be used. Mixtures of any of the above compounds may be employed in the process. The phenol or thiophenol compound may be employed in any suitable amount in the process.
Numerous cyclic organic carbonate compounds may be used in the invention. In general, suitable organic carbonate compounds include any cyclic carbonate having a six-membered ring that is capable of undergoing alkoxylation with an aromatic compound containing an active-hydrogen. Generally, compounds of the formula
where R
1
through R
6
may each independently be hydrogen, or linear or branched alkyl containing from one to six carbons atoms. A preferred configuration is for at least four of the substituents to be hydrogen, and for one of the remaining two substituents to be either methyl or ethyl. Particularly suitable cyclic organic carbonates are any substituted 1,3-dioxan-2-one, such as the 4-, and 5-methyl derivatives (I and II respectively).
The catalyst employed in the alkoxylation reaction may be selected from an alkali metal; an alcohol-derived salt of the alkali metal; alkali metal carbonates; stannates; tertiary amines; quaternary ammonium salts; phosphonium salts; and mixtures of any of these, or any other material capable of catalyzing the reaction.
Nonlimiting examples of specific catalysts include potassium iodide and hydroxide; potassium carbonate; potassium stannate; potassium metal; sodium metal; potassium t-butoxide; triphenylphosphine; tributylphosphine; diphenylbutylphosphine; dibutylphosphine; tetraphenylphosphonium bromide; triphenyl phosphonium acetate; tetrabutylphosphonium bromide; tetrabutylphosphonium acetate; 2-methylimidazole; N-(2′-hydroxyethyl)-2-methylimidazole; piperidine; triethylamine, tributylamine; zinc octoate; magnesium octoate; zirconium hexanoate; dimethyl cyclohexylamine; triethylamine; zinc acetate; and benzotriazole.
The catalyst may be used in various amounts in the process. Typically as is known to one skilled in the art, the preferred amount will vary depending on the type of active-hydrogen species, cyclic organic carbonate, and particular catalyst used. Reaction conditions such as temperature and pressure also may also influence the optimum quantity of catalyst needed. The amount of catalyst is generally any amount between about 0.005 and 3.0 percent by weight based on the total quantity of reaction components. The preferred amount of catalyst is any value between about 0.01 to 1.0 percent by weight.
Additional components that are known to those of skill in the art may be utilized in the process. As an example, the reaction may take place in the presence of an appropriate inert solvent such as, for example, tetrahydronaphthalene; naphthalene; anisole; dimethyl formamide; diethyleneglycol dimethylether (diglyme) and triethyleneglycol dimethylether (triglyme).
The use of a solvent will typically depend on its properties and on the types of active-hydrogen species, cyclic organic carbonate, and catalyst used. Typically, the addition of a solvent is not necessary for carrying out the reaction. Hydroquinone may also be added to the reaction mixture to inhibit polymerization of the cyclic carbonate.
The process may be carried out using various molar ratios of the cyclic organic carbonate compound to the active-hydrogen species. Preferably, the cyclic organic carbonate may be added in excess ranging from about 1.02 to 1.50 moles per every mole of hydroxyl or thiol group present in the active-hydrogen species. More preferably, the excess of cyclic carbonate will be between about 1.05 to 1.25 mole for every mole of hydroxy or thiol group present in the active-hydrogen moieties. In the event that an excess of cyclic organic carbonate compound is used, the amount present after the reaction may optionally be removed by vacuum distillation or other appropriate purification procedure.
The process of the invention may be carried out in any suitable vessel that is constructed to contain the reactants and products. Preferably, the materials of the vessel are inert under the conditions employed during the process. Such materials may include glass, stainless steel, and the like.
The reaction may be run at any suitable temperature, preferably from about 100° C. to 220° C., and more preferably from about 150° C. to 200° C. It is believed that the reaction rate of the alkoxylation reaction is temperature dependent, with faster rates being observed at higher temperatures, and the decomposition of reactants and products likely to occur at higher temperatures.
Clements John H.
Klein Howard P.
Marquis Edward T.
Brown Ron D.
Huntsman Petrochemical Corporation
Lambkin Deborah O.
Stolle Russ R.
Whewell Christopher J.
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