Patent Application
20250002510
Methods of making phosphorous compounds comprising an additional functional group are disclosed. Such compounds can be polymerized to generate proton exchange membranes and/or used in metal bonding.
Because phosphorous and fluorine atoms bring complimentary properties, the combining of these atoms into a molecule can result in synergetic features making them valuable for materials such as ionomeric polymers for use in polymer electrolyte membranes, adhesion promoters, and anticorrosive coatings to name a few.
Ionomeric fluoropolymers comprising both fluorine and phosphorous atoms are typically obtained by direct homopolymerization of monomers bearing both elements, radical copolymerization of fluoroolefins with vinyl monomers containing dialkyl phosphonates, or chemical modification of various types of phosphorous or fluorinated polymers. With respect to monomers bearing a fluorinated olefinic group (especially with more than 2 carbon atoms) and a phosphorous moiety, the methods to produce such monomers are in general very cumbersome involving many steps and/or more elaborate process conditions (such as ultraviolet light or extreme temperatures). For example, EP 0398250 B1 (Tatemoto) describes three different ways to prepare vinylphosphonic acid derivatives. The first preparation reacts tetrafluoroethylene with a trialkyl phosphite at 170° C. for 8 hours. The second preparation involves at least five reaction steps including a pyrolysis at 180-220° C. The third preparation involves at least five reaction steps including heating at 150° C. and the use of peroxides. J. Am. Chem. Soc. 1997, 119, 9137-9143 teaches a method for making (EtO)2P(O)CF2CF═CF2 wherein a diphosphonic acid is contacted with ultraviolet radiation in the presence of an alkenyl iodide followed by a peroxidic oxidation with an isolated yield of 59%.
There is a desire to identify alternative methods of making fluorinated phosphorous-containing compounds. especially phosphorous-containing monomers having a carbon-carbon double bond. The new methods should involve fewer process steps and provide (a) high yields, (b) use reagents that are more readily available and are more environmentally-friendly, (c) minimize the formation of unwanted by-products or phosphoryl chloride, which make isolation difficult, and/or (d) use processes that are more user friendly for large scale processing (such as not relying on radical generation by ultraviolet light or utilizing temperatures below −90° C. or greater than 100° C.).
In one aspect, a method for making a multifunctional compound is disclosed, the method comprising:
CFY1═CF—CF2Y2 or CFY2═CF—CF2Y1
CF2═CF—CFY2—(OR)n—P(═O)(ORh1)2 (IIIA)
CF2X1CF═CF—(OR)n—P(═O)(ORh1)2 (IIIB)
In one embodiment, the third compound from above is silylated to form a fourth compound of the formula
CF2═CF—CFY2—(OR)n—P(═O)(OSiRh23)2 (IVA)
or
CF2X2CF═CF—(OR)n—P(═O)(OSiRh23)2 (IVB)
In another embodiment, the fourth compound from above is transesterified by an alcohol to form a phosphonic acid compound according to the formula
CF2═CF—CFY2—(OR)n—P(═O)(OH)2 (VA)
or
CF2X3CF═CF—(OR)n—P(═O)(OH)2 (VB),
In another aspect, novel compounds according to one of the following formulas are described:
CF2═CF—CFY2—(OR)—P(═O)(OQ)2 (VIIA)
CF2X3CF═CF—(OR)—P(═O)(OQ)2 (VIIB),
CF2X3CHFC(═O)—(OR)—P(═O)(OH)2 (VIB)
In another aspect, the compounds according to formulas (VIIA) and (VIIB) are polymerized to form a polymer, which in one embodiment, may be used in an ion exchange membrane.
In yet another embodiment, compounds according to any one of formulas:
CF2═CF—CFY2—(OR)n—P(═O)(OQ)2 (VIIA)
CF2X3CF═CF—(OR)n—P(═O)(OQ)2 (VIIB),
CF2X3CHFC(═O)—(OR)n—P(═O)(OH)2 (VIB)
The above summary is not intended to describe each embodiment. The details of one or more embodiments of the invention are also set forth in the description below. Other features, objects, and advantages will be apparent from the description and from the claims.
As used herein, the term
Also herein, recitation of ranges by endpoints includes all numbers subsumed within that range (e.g., 1 to 10 includes 1.4, 1.9, 2.33, 5.75, 9.98, etc.).
Also herein, recitation of “at least one” includes all numbers of one and greater (e.g., at least 2, at least 4, at least 6, at least 8, at least 10, at least 25, at least 50, at least 100, etc.).
The present disclosure is directed toward a novel synthesis of phosphate-containing fluorinated compounds comprising an additional functional group. Such a reaction enables the synthesis of a phosphorous salt intermediate which can then be further reacted to form multifunctional compounds, comprising a fluorinated moiety (in some embodiments, a fluorinated alkene moiety) and a phosphorous moiety.
In addition, due to the new synthetic route, additional novel molecules were realized as disclosed herein
In the method of the present disclosure, a first compound represented by formula (I) is combined with a base to form an intermediate, which is then subsequently reacted with a second compound to form Formula (IIA) or (IIB).
The first compound is represented by the formula: H—(OR)n—P(═O)(ORh1)2 (I), wherein n is an integer of 0 or 1; R is a C1-C4 alkenyl group; and Rh1 is a hydrocarbon alkyl group optionally comprising at least one catenated ether linkage. The alkenyl group is a divalent hydrocarbon group comprising 1, 2, 3, or 4 carbon atoms, which may be linear or branched. Exemplary R groups include —CH2—, —(CH2)2—, —(CH2)3—, —(CH2)4—, —CH2(CH3)—, etc. The alkyl group comprises 1, 2, 3, 4, 5, or 6 carbon atoms and may be linear, branched, or cyclic in nature, optionally comprising at least one catenated ether linkage. Exemplary Rh1 groups include: —CH2CH3, —CH2CH2CH3, —CH2CH2CH2CH3, —C(CH3)3, —CH(CH3)2, —c—C6H11, and —(CH2)2—O—CH3. As shown in formula (I) above, the molecule comprises two ORh1 groups, which are typically identical. Molecules according to Formula (I) may be commercially available or synthesized using known processes such as reaction of diethyl hydrogen phosphite with paraformaldehyde and potassium carbonate in alcohol. Exemplary molecules according to Formula (I) are dimethyl hydrogen phosphite, diethyl hydrogen phosphite, dimethyl (hydroxymethyl)phosphonate and diethyl (hydroxymethyl)phosphonate.
A base is used to deprotonate the first compound to form an intermediate salt. Such bases include non-nucleophilic bases known in the art including: alkali and alkaline earth metal hydrides such as sodium hydride, lithium hydride, potassium hydride, calcium hydride, ruthenium hydride and caesium hydride; metal bicarbonates such as sodium bicarbonate and potassium bicarbonate; metal tert-butoxide such as sodium tert-butoxide and potassium tert-butoxide; n-butyl lithium; and strong non-nucleophilic bases such as lithium diisopropylamide, sec-butyllithium, lithium bis(trimethylsilyl)amide, and 1,8-diazabicylco[5.4.0]undec-7-ene. In one embodiment, the strong non-nucleophilic base has a pKa value of its conjugate acid in water of greater than 10.
The first compound is reacted with a base to form an intermediate salt. Typically, this reaction is conducted in a polar aprotic solvent Exemplary solvents that are preferably used are non-reactive organic solvents, including nitriles (such as acetonitrile and propionitrile); ethers (such as tetrahydrofuran, diethylether, and 1,4-dioxane); amides (such as dimethylformamide, dimethylacetamide, and hexamethylphosphoramide); glymes (such as monoglyme, diglyme, tetraglyme, and di(propylene glycol) methylether); lactames (such as N-methylpyrrolidinone); and combinations thereof. In one embodiment, the reaction of the first compound of formula (I) with the base may occur at pressures from at least ambient (1 bar), 3 bar, or even 5 bar to pressures no higher than 10 bar, 15 bar, or even 20 bar. In one embodiment, the reaction of the first compound of formula (I) with the base may occur at temperatures of at least −30, −20, −10, −5, 0, 10, 20, or even 25° C.; and at most 80, 60, 40, or even 35° C. In one embodiment, the molar ratio of the first compound of formula (I) with the base is 20:1 to 1:20, preferably 10:1 to 1:10.
The intermediate salt is then reacted with a second compound represented by the formulas CFY1═CF—CF2Y2 (IIA) or CFY2═CF—CF2Y1 (IIB) where Y1 is a leaving group selected from —F, —I, —Cl, —Br, —OSO2Cl, −OSO2CH3, —OSO2F, or —OSO2CF3 and Y2 is —H, —F, —Cl, —Br, or a fluoroalkyl group. The fluoroalkyl group may comprise a fully fluorinated or partially fluorinated moiety comprising 1, 2, or 3 carbon atoms and optionally comprising an ether linkage and/or at least one of a chlorine, bromine, or iodine substituent. Exemplary second compounds include hexafluoropropylene, 1,1,2,3,3-pentafluoropropene, 3-iodoperfluoropropene, 3-chloroperfluoropropene, 3-bromoperfluoropropene, CF3O—CF═CF—CF3, CF3—O—CF2—CF═CF2, CF3—CF2—O—CF═CF—CF3, CF3—CF2—O—CF2—CF—CF2, CF3—CF3—CF2—O—CF═CF—CF3, CF3—CF3—CF2—O—CF2—CF═CF2, CF2═CFCF2O2SO2CF3, CF2═CFCF2OSO2CH3, CF2═CFCF2OSO2Cl, CF2═CFCF2OSO2F, 1,1,1,2,3-pentafluoropropene, 1-chloroperfluoropropene, 1-bromoperfluoropropene, CF3CF═CFOSO2CH3, and CF3CF═CFOSO2Cl.
Although not wanting to be bound by theory, it is believed that the second compound reacts by nucleophilic addition with the (OR)n—P(═O)(ORh1)2− anion adding to the Y2 side of the double bond in an SN2 type reaction under rearrangement of the double bond and release of the leaving group as shown by the exemplary equation below where Y1 in formula (IIA) is replaced by —OSO2CF3:
The reaction of the second compound with the intermediate is done in solvent under temperatures to form the corresponding third compound represented by formulas CF2—CF—CFY2—(OR)n—P(═O)(ORh1)2 (IIIA) and CF2X1CF═CF—(OR)n—P(═O)(ORh1)2 (IIIB) where X1 is F or —(OR)n—P(═O)(ORh1)2; and R, n, Rh1, Y1, and
The third compound may undergo further processing to obtain a protonated phosphorous moiety. For example, the third compound may be silylated to form a fourth compound of the formulas CF2═CF—CFY2—(OR)n—P(═O)(OSiRh23)2 (IVA) or CF2X2CF═CF—(OR)n—P(═O)(OSiRh23)2 (IVB), where X2 is F or —(OR)n—P(═O)(OSiRh23)2; Rh2 is an alkyl group comprising 1 to 2 carbons; and R, n, and Y2 are the same as described above. Such silylating reactions can include the use of a bromo or chloro trialkylsilane to replace the Rh1 group in Formulas (IIIA) and (IIIB) with a trialkyl silyl group (e.g., —SiRh23).
Typically, this silylation reaction is not conducted in a solvent. In one embodiment, the mole ratio of the third compound to the silylating agent is 1:5 to 5:1, preferably 3:1 to 1:3. In one embodiment, the silylation reaction may occur at pressures from at least ambient (1 bar), 3 bar, or even 5 bar to pressures no higher than 10 bar, 15 bar, or even 20 bar. In one embodiment, the silylation reaction may occur at temperatures of at least −30° C. 0° C., 20° C., or even 25° C.; and at most 80° C., 50° C., or even 35° C.
The fourth compound may then be reacted to yield a fifth compound of the formulas CF2═CF—CFY2—(OR)n—P(═O)(OH)2 (VA) or CF2X3CF═CF—(OR)n—P(═O)(OH)2 (VB), which is a phosphonic acid. In Formulas (VA) and (VB), X3 is F or
The reaction of the fourth compound of Formula (IVA) to yield the fifth compound (VA) is as follows:
CF2═CF—CFY2—(OR)n—P(═O)(OSiRh23)2+alcohol (dry)→CF2═CF—CFY2—(OR)n—P(═O)(OH)2
This reaction will be referred to herein under the general term “transesterification” to describe the transformation of one ester into another ester through the interchange of the alkoxy moiety.
Typically, this transesterification reaction is conducted at temperatures of at least −30° C., 0° C., 10° C., or even 15° C.; and at most 30° C., 20° C., or even 25° C. In one embodiment, the transesterification reaction is conducted at pressures from at least ambient (1 bar), 3 bar, or even 5 bar to pressures no higher than 10 bar, 15 bar, or even 20 bar. Typically, to achieve high yield, an excess of the alcohol is used for example the molar ratio of the fourth compound to the alcohol is 1:1 to 1:200, preferably 1:1 to 1:100. In one embodiment, a catalyst (such as a strong acid or base) may be used to favor product formation.
The process as described above can make ionomer precursors or monomers such as (HO)2P(═O)—CF2CF═CF2; (HO)2P(═O)—CH2OCF2CF═CF2; (HO)2P(═O)—CH2OCF═CFCF3; and salts thereof.
In one embodiment, if the alcohol used in the transesterification reaction described above is not dry (i.e., free of water), the fourth compound can undergo a hydrolysis wherein Formula (IVB) is converted to a compound according to Formula (VIB):
It is to be appreciated that the multifunctional compounds of the present disclosure may include the cis isomer, the trans isomer, or a mixture of cis and trans isomers.
It should also be appreciated that the phosphonic acid groups in the reaction products may be exchanged using standard chemistry practices to convert the acid into a corresponding salt. In one embodiment, the counter ion is organic, such as an alkylammonium (e.g., tetramethylammonium, tetrabutylammonium, etc.). In another embodiment, the counter ion is inorganic, such as an ammonium, or a metal, such as alkali metal (e.g., Na, K, Li, etc.) or alkaline earth metal (e.g., Mg, Ca, etc.).
The molecules as made by the processes disclosed herein may be subsequently purified for use to isolate the desired compound. Purification can be done by conventional means including distillation, absorption, extraction, chromatography and recrystallization. The purification can be done to isolate the desired compound of the present disclosure (in all its distereoisomeric forms) from impurities, such as starting materials, byproducts, etc. The term “purified form” as used herein means the desired compound is at least 90, 95, 98, or even 99 wt % pure.
As discussed above and exemplified below, the generation of phosphorous-containing monomers having a carbon-carbon double bond can be achieved in as few as two to three process steps, none of which require ultraviolet radiation or temperatures above 100° C. As shown in the examples below isolated yields of at least 65, 70, 75, or even 80% can readily be achieved, without the use of chlorofluorocarbon based solvents nor the generation of phophoryl chlorides.
As disclosed above, a number of molecules may be synthesized using the processes disclosed herein. In one embodiment, the present disclosure is directed toward novel compounds such as those shown by Formula (VIB) CF2X3CFHC(═O)(OR)n—P(═O)(OH)2, Formula (VIIA) CF2═CF—CFY2—OR—P(═O)(OQ)2, or Formula (VIIB) CF2X3CF═CF—OR—P(═O)(OQ)2 where R is a C1-C4 alkenyl group; X3 is F or —(OR)n—P(═O)(OQ)2;Y2 is —F, —Cl, —Br, —H, or a fluoroalkyl group; and Q is an alkyl group having 1 to 6 carbon atoms and optionally comprising at least one catenated ether linkage, —Si(CH3)3, —Si(CH2CH3)3, —H, a metallic cation, or a quaternary ammonium cation.
Exemplary molecules include: (QO)2P(═O)—(RO)n—CF2CF—CFO—(RO)n—P(═O)(OQ)2, wherein R is a C1-C4 alkenyl group, n is 0 or 1, and Qis an alkyl group having 1 to 6 carbon atoms and optionally comprising at least one catenated ether linkage, —Si(CH3)3, —Si(CH2CH3)3, —H, a metallic cation, or a quaternary ammonium cation. Such molecules include tetralkyl {[(1E and 1Z)-perfluoropropenyl-1,3-diyl]bis(oxymethylene)}bis(phosphonate).
Exemplary molecules include: (QO)2P(═O)—(RO)n—CF2CF—CF2 wherein R is a C1-C4 alkenyl group. n is 0 or 1, and Q is an alkyl group having 1 to 6 carbon atoms and optionally comprising at least one catenated ether linkage, —Si(CH3)3, —Si(CH2CH3)3, —H, a metallic cation, or a quaternary ammonium cation. Such a molecule includes: dialkyl{[(1,1,2,3,3-pentafluoroprop-2-en-1-yl)oxy]methl}phosphonate.
Exemplary molecules include: (QO)2P(═O)—(RO)n—CF—CFCF3 wherein R is a C1-C4 alkenyl group, n is 0 or 1, and Q is an alkyl group having 1 to 6 carbon atoms and optionally comprising at least one catenated ether linkage, —Si(CH3)3, —Si(CH2CH3)3, —H, a metallic cation, or a quaternary ammonium cation. Such molecules include: ({[(1E and 1Z)-perfluoropropenyl-oxy}methyl)phosphonic acid.
In one embodiment, the multifunctional molecules disclosed herein can be useful in electrochemical cells (e.g., fuel cell, redox flow battery, etc.). Electrochemical devices, including proton exchange membrane fuel cells (PEMFCs), sensors, electrolyzers, chlor-alkali separation membranes, redox flow batteries, and the like, typically comprise an ion conducting membrane or polymer electrolyte membrane sandwiched between two electrodes. a cathode and an anode. The membrane and the two electrodes are sandwiched between current collector plates, which optionally have a field flow pattern etched thereon, and then held together such that each layer is in contact, preferably intimate contact with the adjacent layers to form an electrochemical cell. Charge movement between the anode and cathode enables the electrochemical device.
In one embodiment, the monomers as disclosed herein may be useful in generating ionomeric polymers, which may be used in electrochemical cells. In one embodiment, the phosphorous-containing compounds disclosed herein comprising a double bond are interpolymerized to form a homopolymer. In another embodiment, the ionic fluorinated polymer is derived from the interpolymerization of the phosphorous-containing compounds disclosed herein comprising a double bond with fluorinated monomers including tetrafluoroethylene, hexafluoropropylene, vinyl fluoride, vinylidene fluoride, fluorinated ether monomers (for example, perfluoro (methyl vinyl) ether, perfluoro (ethyl vinyl) ether, perfluoro (n-propyl vinyl) ether, perfluoro-2-propoxypropylvinyl ether, perfluoro-3-methoxy-n-propylvinyl ether, etc.) and other fluorinated monomers as known in the art. Polymerization techniques of these particular monomers would be similar to those techniques known in the art.
The ionic fluorinated polymer may be cast or processed into an ion exchange membrane. For example, the ionic fluorinated polymer may be formed into a liquid composition, which is subsequently cast or imbibed into a support (such as porous polytetrafluoroethylene) to generate a membrane. In one embodiment, the resulting polymer electrolyte membrane has a thickness of at most 200, 90, 60, or even 40 micrometers, and at least 10, 15, 20, 35, 30, or even 35 micrometers
The ionomeric polymer and/or the resulting polymeric electrolyte membrane should be sufficiently conductive for use in electrochemical cells. In one embodiment, when measured in the acid form (e.g., the ionic fluorinated polymer in its acid form, or the polymer electrolyte membrane in its acid form), the ionic fluorinated polymer and/or the resulting polymeric electrolyte membrane has a conductivity of at least 1, 10, 20, or even 30 mS/cm and at most 50, 60, 70, 80, 90, 100 or even 200 mS/cm (milliSiemens per centimeter) at 50% relative humidity (RH) and 80° C.
In one embodiment, the ionic fluorinated polymer made from the multifunctional
monomers disclosed herein has an equivalent weight (EW) of at least 200, 700, or even 800, and at most 1500, 1200, 1100, 1000, or even 900 grams/mole.
Because of the good bonding of the phosphorous-containing moiety to other metals, the compounds disclosed herein (or polymers therefrom) can be used to improve the adhesion of fluorinated compositions to metal substrates.
In one embodiment, the multifunctional compounds as disclosed herein (or polymers therefrom) may be used to facilitate adhesion within the electrochemical cell. For example, in one embodiment, the multifunctional compounds disclosed herein can be contacted with catalyst particles comprising metals such as platinum, ruthenium or iridium, which are used in an anode and/or cathode. The multifunctional compounds would allow good bonding of fluorinated moieties to these metal catalyst particles in wet and dry conditions, thus increasing the durability of the electrodes.
In another embodiment, the multifunctional compounds as disclosed herein (or polymers therefrom) could improve bonding of the polymer electrolyte membrane to metallic current collector plates, such that the overall sealing in the electrochemical cell is improved, since no gases will be able to escape out of the electrochemical cell in a lateral direction.
Advantageously, because of the chelating ability of phosphonic acid or salt thereof, the presence of the multifunctional compounds as disclosed herein (or polymers therefrom) in electrochemical cells may be used as radical scavengers, helping to bind cerium, manganese, or other species. Because the phosphonic acid moiety (or salt thereof) in the present disclosure is on a molecule that can be polymerized, these radical scavengers can be immobilized, preventing the radical scavengers and/or the radical scavenger/radical complex from being moved within and/or away from the electrochemical cell.
In another embodiment, the multifunctional compounds of the present disclosure (or polymers therefrom) can be used to improve the performance of a lithium ion battery. For example, fluoropolymers do not have good bonding to the Al charge collector (cathode) or Cu charge collector (anode) in lithium ion batteries. The multifunctional compounds of the present disclosure, which comprise a phosphorous group and a fluorinated moiety, can be used to improve the bonding of the cathode and the anode to the charge collector. This improved bonding can result in better cycle stability and capacity retention of the electrodes and lithium ion battery.
The ability of the compounds disclosed herein to chelate metal and bond to metals may engender these compounds (or polymers therefrom) to be used in other applications besides electrochemical cells. In one embodiment, the compounds disclosed herein may be used as a chelating agent for (rare) earth metal recovery. In one embodiment, the compounds disclosed herein can be adsorbed directly onto a metal surface enabling the fluorinated portion of the compound to face away from the surface, generating a surface layer sufficiently bonded to the metal surface, which is resistant to chemical attack.
Advantages and embodiments of this disclosure are further illustrated by the following examples, but the particular materials and amounts thereof recited in these examples, as well as other conditions and details, should not be construed to unduly limit this invention. In these examples, all percentages, proportions and ratios are by weight unless otherwise indicated.
Unless otherwise noted or readily apparent from the context, all parts, percentages, ratios, etc. in the Examples and the rest of the specification are by weight. The following abbreviations are used in this section: eq=equivalents, min=minutes, h=hours, RT=room temperature, mol=moles, mmol=millimoles, mL=milliliters, L=liters, g=grams, M=molar, mbar=millibar, equiv=equivalents, NMR=nuclear magnetic resonance, b.p.=boiling point.
Paraformaldehyde (36.6 g, 1.2 mol), potassium carbonate (6.4 g, 46.6 mmol), and ethanol (700 mL) were added under inert atmosphere to a three-necked flask (1 L) equipped with a thermometer and reflux condenser. The suspension was stirred vigorously for 1.5 h at RT and diethyl phosphite (128.5 g, 0.9 mol, 120 mL) was quickly added. The reaction mixture was heated to 72 to 73° C. and stirred at this temperature over the course of 18 h. Then, the reaction mixture was cooled to room temperature, filtered and the solvent was evaporated in vacuo. The crude product was distilled via a Vigreux column in vacuo (7 mbar). The desired product was obtained as a clear colorless liquid with b.p. 105 to 109° C. at 7 mbar. The yield was 78% (113.6 g, 0.7 mol). The structure assigned was consistent with spectral analysis.
PFAFS was prepared following the procedure described in Molecules 2011, 16, 6512-6540.
PFAI were prepared following the procedure described in Molecules 2011, 16, 6512-6540.
A suspension of NaH in mineral oil (6.1 g, 153.0 mmol, 1.06 equiv.; 60%) and dry CH3CN (85 mL) were added to a 250 mL three-necked flask equipped with a thermometer and reflux condenser. The suspension was stirred for 20 min at room temperature, then cooled to 18° C. and diethyl phosphite (20.0 g, 145.0 mmol) was slowly added dropwise at this temperature so that the reaction temperature did not exceed 31° C.
Then, the reaction mixture was stirred over 3.5 h until the reaction mixture got transparent. The reaction mixture was transferred into a 250 mL dropping funnel under inert gas atmosphere. The dropping funnel was connected to a 250 mL three-necked flask equipped with a thermometer and a reflux condenser. Perfluoro allyl fluorosulfate (PE-2:36.7 g, 159.6 mmol, 1.1 equiv.) and dry CH3CN (75 mL) were added to this flask and the reaction solution was cooled to −30° C.
At this temperature, the salt solution was added to the solution of PFAFS. During the addition, the reaction temperature rose to −20° C. The reaction mixture was stirred at this temperature for 2.5 h, slowly warmed to room temperature and allowed to stir at this temperature over the course of 15 h. Afterwards, the reaction mixture was evaporated in vacuo and carefully poured into a solution of ice-cold hydrochloric acid (250 mL 3%). The water phase was extracted with diethyl ether (3×200 mL). The organic phases were combined, washed with a cold aqueous saturated sodium chloride solution (1×300 mL) and saturated NaHCO3 (3×300 mL), and dried thoroughly with anhydrous magnesium sulfate. The solvent was evaporated in vacuo.
The crude product was distilled over a short Vigreux column in vacuo (0.7 mbar). PADP was isolated as clear yellowish liquid in 68% yield (26.3 g, 98 mmol, b.p. 49 to 51° C. at 0.7 mbar) and the spectral analysis was consistent with the PADP structure.
Ex-1 (20.2 g, 75.4 mmol) was added under inert atmosphere to a 100 mL three-necked flask equipped with a thermometer and reflux condenser.
The starting compound was cooled to 10° C. and bromotrimethylsilane (30.0 g, 196.1 mmol, 2.6 equiv.) was quickly added. The reaction mixture was stirred intensively at 45 to 46° C. over the course of 1 h and at 65° C. for a further 18 h. After cooling to room temperature, the reaction mixture was evaporated in vacuuo (0.7 mbar) at 30 to 31° C. within 3 h.
Bis(trimethylsilyl) (1,1,2,3,3-pentafluoroprop-2-en-1-yl)phosphonate was isolated in 96% yield (25.8 g, 72.5 mmol) as an oily residue with traces of bis(trimethylsilyl) phosphorofluoridate. Spectral analysis was consistent with the bis(trimethylsilyl) (1,1,2,3,3-pentafluoroprop-2-en-1-yl)phosphonate structure.
In a 500 mL three-necked flask, equipped with a thermometer and reflux condenser, Ex-2 (25.5 g, 71.6 mmol) was dissolved in methanol (200 mL) at room temperature under an argon atmosphere and water (40.0 g, 2.2 mol, 31.0 equiv.) was added dropwise so that the reaction temperature did not exceed 30° C.
Then, the reaction mixture was stirred intensively at a temperature of 25 to 30° C. over 48 hours. At the end of the reaction, the reaction mixture was concentrated in vacuo, the residue was dissolved in water (150 mL) and extracted with diethyl ether (3×150 mL).
The water solution was concentrated by a water-jet pump at 40° C. and the liquid residue was dried thoroughly in vacuo (0.7 mbar) at 35° C. within 5 h. The yield of (1,1,2,3,3-pentafluoroprop-2-en-1-vl) phosphonic acid (PAPA) was 82% (12.6 g. 59 mmol). Spectral analysis was consistent with the PAPA structure.
A suspension of sodium hydride in mineral oil (60%; 3.4 g, 85.0 mmol) and tetrahydrofuran (THF; 270 mL) were added to a three-necked flask (500 mL) equipped with a dropping funnel, thermometer, and reflux condenser. The suspension was stirred for 15 min at RT, then cooled to 5° C. and PE-1 (13.3 g, 79.1 mmol) was slowly added to the flask. Then, the reaction mixture was stirred for 2 h at this temperature and within 1.5 h warmed up to 18° C. until the reaction mixture was almost transparent. The reaction solution was cooled to −75° C. The dropping funnel was replaced by a gas inlet tube and hexafluoropropene (HFP; 33.6 g, 224.0 mmol) was added at −75 to −65° C. so that the reaction temperature of −62° C. was not exceeded and HFP was completely liquefied. The reaction mixture was stirred at this temperature for 1 h and allowed to stir overnight while slowly warming up to room temperature. A saturated NH4Cl solution (61 mL) was carefully added to the reaction mixture under vigorous stirring at RT. The lower layer was separated, and the water phase was extracted with diethyl ether (3×100 mL). The organic phases were combined, washed with an aqueous saturated sodium chloride solution and then thoroughly dried with anhydrous sodium sulfate. The solvent was evaporated in vacuo. The remaining residue was collected and distilled via a Vigreux column in vacuo (7 mbar). The desired olefin as a mixture of cis and trans isomers (22 mol % to 78 mol %) was a clear, colorless liquid with b.p. 71 to 75° C. at 7 mbar. The yield was 98% (23.4 g. 78 mmol). The trans and cis isomers mentioned above were consistent with the spectral analysis.
Diethyl ({[(1E & 1Z)-1,2,3,3,3-pentafluoroprop-1-en-1-yl]oxy}methyl)phosphonate (cis/trans-mixture) prepared as described for EX-4 (6.4 g. 21.5 mmol) was placed in a three-necked flask (50 mL) equipped with a thermometer and reflux condenser under inert atmosphere. The starting compound was cooled to 12° C. and bromo trimethylsilane (9.6 g, 62.7 mmol) was rapidly added. The reaction mixture was stirred vigorously at 40°° C. over the course of 1 h and at 50° C. for further 18 h. After cooling to room temperature, the reaction mixture was concentrated in vacuo (21 mbar) at 35 to 45° C. for 1.5 h and at RT at 7 mbar for 3 h.
The product was isolated in 98% yield (8.1 g, 21.0 mmol) and characterized with 1H NMR (401 MHz, CDCl3), 13C NMR (101 MHz, CDCl3), 19F NMR (376 MHz, CDCl3), and 31 P{1H} NMR (161 MHZ, CDCl3) analysis.
The product from EX-5 (8.1 g, 21.0 mmol) was poured into methanol (70 mL) in a three-necked flask (100 mL) equipped with a thermometer and reflux condenser under inert gas atmosphere at RT. Water (10 g) was carefully added under vigorous stirring so that the reaction temperature did not exceed 29° C.
The reaction mixture was stirred intensively at RT for 48 h. At the end of the reaction, the reaction mixture was evaporated in vacuo at 40° C. The residue was dissolved in acetone (100 mL) and then thoroughly dried with anhydrous MgSO4. The acetone solution was filtered, evaporated and the liquid residue was dried thoroughly in vacuo (7 mbar) at 35 to 40° C. over the course of 3 h. The yield was 97% (4.9 g; 20.4 mmol). Spectral analysis was consistent with the above-listed structure.
Bis(trimethylsilyl) ({[(1E& IZ)-1,2,3,3,3-pentafluoroprop-1-en-1-y]oxy}methyl)phos-phonate (as made in EX-5 including both cis and trans forms, 44.2 g, 114.4 mmol) was added under inert atmosphere to a three-necked flask (1 L) equipped with a thermometer and reflux condenser. Under vigorous stirring, methanol (800 mL) was quickly added so that the reaction temperature did not exceed 25° C. Afterwards, the reaction mixture was stirred for two days at RT. At the end of the reaction, the mixture was concentrated at 35° C. in vacuo and the liquid residue was thoroughly dried in vacuo (7 mbar) at room temperature over the course of 2.5 h. The yield was 97% (26.8 g, 110.7 mmol). Spectral analysis was consistent with the above-listed structures.
A suspension of sodium hydride in mineral oil (60%, 1.6 g, 40.0 mmol) and monoglyme (70 mL) were added to a three-necked flask (100 mL) equipped with a dropping funnel, thermometer and reflux condenser. The suspension was stirred 0.5 h at RT, then cooled to 5° C. and PE-1 (6.3 g, 37.5 mmol) was slowly added to the flask so that the reaction temperature did not exceed 8° C. The reaction mixture was slowly warmed up to 15° C. and stirred at this temperature over the course of 2.5 h until it became almost transparent. Then, the reaction mixture was cooled to −60° C. and perfluoroallyl iodide (PFAI; 9.6 g, 37.2 mmol) was slowly added. The reaction mixture was slowly warmed up to RT, stirred for 48 h, was filtered, concentrated in vacuo and carefully poured into ice-cold water (150 mL) and extracted with chloroform (3×100 mL). The organic phases were combined, washed with cold water (3×150 mL) and a saturated NaHCO3 solution (200 mL) and then dried thoroughly with anhydrous magnesium sulfate. The solvent was evaporated in vacuo. The remaining residue was distilled via a Vigreux column in vacuo (7 mbar). The desired olefin was obtained as a clear yellowish liquid with b.p. 64 to 68° C. at 7 mbar. The yield was 11% (1.2 g, 4.0 mmol). Spectral analysis was consistent with the Diethyl {[(1,1,2,3,3-pentafluoroprop-2-en-1-vl)oxy]methyl}phosphonate structure.
A three-necked flask (100 mL) equipped with a dropping funnel, thermometer and reflux condenser was charged with diethyl ether (65 mL) and cooled to −80° C. Afterwards, a solution of butyllithium (n-BuLi) in n-hexane (2.5 M: 10.6 g, 38.1 mmol, 1 eq.) was added. The solution was cooled to −90° C. and diethylhydroxymethylphosphonate (6.4 g, 38.1 mmol) was slowly added to the flask so that the reaction temperature did not exceed −85° C. After 1 h, the reaction mixture was warmed up to RT within 1.5 h. The obtained lithium salt solution was transferred to a dropping funnel (100 mL) under inert conditions. The dropping funnel was connected to a three-necked flask (250 mL) equipped with a dropping funnel, thermometer and reflux condenser. The flask was charged with a solution of PE-2 (13.1 g. 56.9 mmol, 1.5 eq.) in diethyl ether (120 mL) and cooled to −20° C. Then, the prior obtained lithium salt solution was added and the reaction temperature increased to −10° C. Afterwards, the reaction mixture was warmed up to RT and a saturated solution of NH4Cl (45 mL) was added. The lower phase was separated, and the aqueous phase extracted with diethyl ether (2×50 mL). The organic phases were combined, washed with water (2×70 mL), aqueous saturated sodium chloride solution (70 mL), and dried with sodium sulfate. The solvent was evaporated in vacuo. The remaining residue was distilled via a Vigreux column in vacuo (7 mbar). The desired olefin was obtained as a clear yellowish liquid with b.p. 65 to 68° C. at 7 mbar. The yield was 47% (5.3 g, 18 mmol).
A suspension of sodium hydride in mineral oil (60%, 1.6 g, 40.0 mmol) and monogly (45 mL) were added to a three-necked flask (100 mL) equipped with a thermometer and reflux condenser. The suspension was stirred for 30 min at room temperature, then cooled to 10 to 12° C. and PE-1 (6.2 g, 36.9 mmol) was slowly added so that the reaction temperature did not exceed 15° C. The reaction mixture was stirred over the course of 2 h until the reaction mixture got transparent and the reaction temperature rose to 20° C. The sodium salt solution was carefully poured into a dropping funnel (100 mL) under inert gas atmosphere, which was connected to a three-necked flask (100 mL) equipped with a thermometer and reflux condenser. PE-2 (4.3 g,18.7 mmol) and MG (25 mL) were added to this flask and the reaction solution was cooled to −35 to −30° C. The salt solution was slowly added at this temperature and the temperature rose to −20° C. Afterwards, the reaction mixture was slowly warmed to RT and was stirred overnight. Then, the reaction mixture was filtered, concentrated in vacuo, and carefully poured into ice-cold water (200 mL) and extracted with chloroform (3×100 mL). The organic phases were combined, washed with cold water (2×200 mL) and a saturated NaHCO3 solution (3×150 mL) and then thoroughly dried with anhydrous magnesium sulfate. The solvent was evaporated in vacuo. The crude product was distilled via a Vigreux column in vacuo (7 mbar). The desired olefin was obtained as a clear yellowish liquid and as a mixture of cis (63%) and trans (37%) isomers with b.p. 161 to 165° C. (7 mbar). Spectral analysis was consistent with the above-mentioned structures.
Foreseeable modifications and alterations of this invention will be apparent to those skilled in the art without departing from the scope and spirit of this invention. This invention should not be restricted to the embodiments that are set forth in this application for illustrative purposes.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IB2022/060291 | 10/26/2022 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 63276681 | Nov 2021 | US |
