Compositions and methods for hydrocarbon functionalization
US-2017152207-A1 · Jun 1, 2017 · US
US12559448B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12559448-B2 |
| Application number | US-202017438091-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 13, 2020 |
| Priority date | Mar 13, 2019 |
| Publication date | Feb 24, 2026 |
| Grant date | Feb 24, 2026 |
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In one aspect, the disclosure relates to a method for functionalizing hydrocarbons. In a further aspect, the method involves heating a hydrocarbon with a composition having an acid and an oxidant. In other aspects, the composition can further include an iodine-based compound and/or a compound having formula AaXn. In any of these aspects, the oxidant can be regenerated in situ or in a separate regeneration step. Also disclosed are functionalized hydrocarbons produced by the disclosed method. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present disclosure.
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What is claimed is: 1 . A method comprising mixing a hydrocarbon with a composition comprising an acid and an oxidant comprising a manganese compound, to produce a functionalized hydrocarbon, wherein the acid is selected from the group consisting of trifluoroacetic acid, triflic acid, trifluoromethyl phosphonic acid, hexafluorobutyric acid, sulfuric acid, acetic acid, methanesulfonic acid, phosphoric acid, and any combination thereof, and the manganese compound is not Mn 2 O 3 , wherein the manganese compound comprises Mn 2 (TFA) 4 (HTFA) 4 . 2 . The method of claim 1 , wherein the composition further comprises iodine, an iodine-based compound, or a combination thereof. 3 . The method of claim 2 , wherein the iodine-based compound comprises iodate, periodate, iodine oxide, iodosyl (IO + ), trivalent iodine compound, or any combination thereof. 4 . The method of claim 2 , wherein the iodine-based compound is Q(IO 3 ) p , wherein Q is hydrogen, lithium, sodium, potassium, beryllium, magnesium, calcium, strontium, barium, transition metals, aluminum, gallium, thallium, indium, tin, sulfur, ammonium (NH 4 + ), alkylammonium, phosphonium (PH 4 + ), alkylphosphonium, arylphosphonium, or trimethyl sulfonium ([S(CH 3 ) 3 ] + ), wherein p is from 1 to 5. 5 . The method of claim 2 , wherein the iodine-based compound is selected from the group consisting of: KlO 3 , Ca(IO 3 ) 2 , Ba(IO 3 ) 2 , Cu(IO 3 ) 2 , NH 4 IO 3 , H 5 IO 6 , KlO 4 , NaIO 4 , NH 4 IO 4 , I(TFA) 3 , I 2 O 5 , [IO] + , [IO 2 ] + , and any combination thereof. 6 . The method of claim 2 , wherein the molar ratio of the oxidant to the iodine or iodine-based compound is from 1:1 to 30:1. 7 . The method of claim 1 , wherein the acid comprises trifluoroacetic acid. 8 . The method of claim 1 , wherein the hydrocarbon and composition are heated at a temperature of from about 100° C. to about 300° C. 9 . The method of claim 1 , wherein the hydrocarbon comprises a linear or branched alkane or a cycloalkane. 10 . The method of claim 1 , wherein the hydrocarbon comprises methane, ethane, or propane. 11 . The method of claim 1 , wherein the hydrocarbon is monofunctionalized. 12 . A method comprising mixing a hydrocarbon with a composition comprising an acid and an oxidant comprising Mn 2 (TFA) 4 (HTFA) 4 to produce a functionalized hydrocarbon. 13 . The method of claim 12 , wherein the acid comprises trifluoroacetic acid, triflic acid, trifluoromethyl phosphonic acid, hexafluorobutyric acid, sulfuric acid, acetic acid, methanesulfonic acid, phosphoric acid, or any combination thereof. 14 . The method of claim 12 , wherein the hydrocarbon comprises a linear or branched alkane or a cycloalkane. 15 . The method of claim 12 , wherein the hydrocarbon comprises methane, ethane, or propane. 16 . The method of claim 12 , wherein the composition further comprises iodine, an iodine-based compound, or a combination thereof. 17 . The method of claim 16 , wherein the iodine-based compound comprises iodate, periodate, iodine oxide, iodosyl (IO + ), trivalent iodine compound, or any combination thereof. 18 . The method of claim 16 , wherein the iodine-based compound is Q(IO 3 ) p , wherein Q is hydrogen, lithium, sodium, potassium, beryllium, magnesium, calcium, strontium, barium, transition metals, aluminum, gallium, thallium, indium, tin, sulfur, ammonium (NH 4 + ), alkylammonium, phosphonium (PH 4 + ), alkylphosphonium, arylphosphonium, or trimethyl sulfonium ([S(CH 3 ) 3 ] + ), wherein p is from 1 to 5. 19 . The method of claim 16 , wherein the iodine-based compound is selected from the group consisting of: KlO 3 , Ca(IO 3 ) 2 , Ba(IO 3 ) 2 , Cu(IO 3 ) 2 , NH 4 IO 3 , H 5 IO 6 , KlO 4 , NaIO 4 , NH 4 IO 4 , I(TFA) 3 , I 2 O 5 , [IO] + , [IO 2 ] + , and any combination thereof. 20 . The method of claim 12 , wherein the composition further comprises A a X n , wherein A is hydrogen, lithium, sodium, potassium, beryllium, magnesium, calcium, strontium, barium, transition metals, aluminum, gallium, thallium, indium, tin, sulfur, ammonium (NH 4 + ), alkylammonium, phosphonium (PH 4 + ), alkylphosphonium, arylphosphonium, trimethyl sulfonium ([S(CH 3 ) 3 ] + ) or a combination thereof, wherein X is chlorine, wherein subscript “a” is an oxidation state of X and subscript “n” is an oxidation state of A. 21 . The method of claim 20 , wherein AX is HCl, NaCl, KCl, CaCl 2 ), LiCl, ZnCl 2 , BeCl 2 , MgCl 2 , NH 4 Cl, transition metal chlorides, or any combination thereof.
by substitution of hydrogen atoms by nitro groups · CPC title
of esters of organic acids · CPC title
of hydrogen atoms (combined with addition of halogens to unsaturated hydrocarbons C07C17/06) · CPC title
by reacting carboxylic acids or symmetrical anhydrides with saturated hydrocarbons · CPC title
of a saturated carbon skeleton · CPC title
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