IL130705A - Hydrogenation of cyanophosphate history - Google Patents
Hydrogenation of cyanophosphate historyInfo
- Publication number
- IL130705A IL130705A IL13070597A IL13070597A IL130705A IL 130705 A IL130705 A IL 130705A IL 13070597 A IL13070597 A IL 13070597A IL 13070597 A IL13070597 A IL 13070597A IL 130705 A IL130705 A IL 130705A
- Authority
- IL
- Israel
- Prior art keywords
- cyanophosphonate
- acid
- derivative
- catalyst
- reaction mixture
- Prior art date
Links
- UCDHYFZYUGDETN-UHFFFAOYSA-N cyanophosphonic acid Chemical class OP(O)(=O)C#N UCDHYFZYUGDETN-UHFFFAOYSA-N 0.000 title claims abstract description 63
- 238000005984 hydrogenation reaction Methods 0.000 title claims description 20
- 238000000034 method Methods 0.000 claims abstract description 73
- MGRVRXRGTBOSHW-UHFFFAOYSA-N (aminomethyl)phosphonic acid Chemical class NCP(O)(O)=O MGRVRXRGTBOSHW-UHFFFAOYSA-N 0.000 claims abstract description 43
- 239000003054 catalyst Substances 0.000 claims abstract description 30
- 239000011541 reaction mixture Substances 0.000 claims abstract description 23
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 20
- 239000001257 hydrogen Substances 0.000 claims abstract description 20
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 23
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 21
- -1 cyanophosphonate diester Chemical class 0.000 claims description 17
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 16
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 claims description 16
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 14
- 150000001875 compounds Chemical class 0.000 claims description 14
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 13
- 238000006243 chemical reaction Methods 0.000 claims description 13
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims description 12
- 150000008064 anhydrides Chemical class 0.000 claims description 11
- FBEIPJNQGITEBL-UHFFFAOYSA-J tetrachloroplatinum Chemical group Cl[Pt](Cl)(Cl)Cl FBEIPJNQGITEBL-UHFFFAOYSA-J 0.000 claims description 11
- 230000015572 biosynthetic process Effects 0.000 claims description 10
- 229910000564 Raney nickel Inorganic materials 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 8
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 8
- 239000007868 Raney catalyst Substances 0.000 claims description 8
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical group [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 claims description 8
- 239000002904 solvent Substances 0.000 claims description 8
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims description 6
- 230000003197 catalytic effect Effects 0.000 claims description 5
- 239000010941 cobalt Substances 0.000 claims description 5
- 229910017052 cobalt Inorganic materials 0.000 claims description 5
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical group [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 5
- 150000007522 mineralic acids Chemical class 0.000 claims description 5
- 229910052697 platinum Inorganic materials 0.000 claims description 5
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 4
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 claims description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 4
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 claims description 4
- 150000007524 organic acids Chemical class 0.000 claims description 4
- XLHJWKVWGSPYGX-UHFFFAOYSA-L dipotassium;phosphonatoformonitrile Chemical compound [K+].[K+].[O-]P([O-])(=O)C#N XLHJWKVWGSPYGX-UHFFFAOYSA-L 0.000 claims description 3
- JJWLVOIRVHMVIS-UHFFFAOYSA-O isopropylaminium Chemical compound CC(C)[NH3+] JJWLVOIRVHMVIS-UHFFFAOYSA-O 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- 150000001408 amides Chemical class 0.000 claims description 2
- KCDPDMXLIRWFCN-UHFFFAOYSA-N cyano(ethoxy)phosphinic acid Chemical compound CCOP(O)(=O)C#N KCDPDMXLIRWFCN-UHFFFAOYSA-N 0.000 claims description 2
- ONAKXHJEGDNSHU-UHFFFAOYSA-N cyano(methoxy)phosphinic acid Chemical compound COP(O)(=O)C#N ONAKXHJEGDNSHU-UHFFFAOYSA-N 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- ANJJMUYMRQDKKX-UHFFFAOYSA-N dicyanophosphoryl dihydrogen phosphate Chemical compound OP(O)(=O)OP(=O)(C#N)C#N ANJJMUYMRQDKKX-UHFFFAOYSA-N 0.000 claims description 2
- XBPCUCUWBYBCDP-UHFFFAOYSA-O dicyclohexylazanium Chemical compound C1CCCCC1[NH2+]C1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-O 0.000 claims description 2
- ZWWWLCMDTZFSOO-UHFFFAOYSA-N diethoxyphosphorylformonitrile Chemical compound CCOP(=O)(C#N)OCC ZWWWLCMDTZFSOO-UHFFFAOYSA-N 0.000 claims description 2
- LPMHDYUMNBBOKR-UHFFFAOYSA-N dimethoxyphosphorylformonitrile Chemical compound COP(=O)(OC)C#N LPMHDYUMNBBOKR-UHFFFAOYSA-N 0.000 claims description 2
- 235000011180 diphosphates Nutrition 0.000 claims description 2
- QFXVYASTPGEDHM-UHFFFAOYSA-L disodium;phosphonatoformonitrile Chemical group [Na+].[Na+].[O-]P([O-])(=O)C#N QFXVYASTPGEDHM-UHFFFAOYSA-L 0.000 claims description 2
- RPFKWRCJNFJETQ-UHFFFAOYSA-M lithium;cyano(ethoxy)phosphinate Chemical compound [Li+].CCOP([O-])(=O)C#N RPFKWRCJNFJETQ-UHFFFAOYSA-M 0.000 claims description 2
- XYNYNGGQGKVHLU-UHFFFAOYSA-M lithium;cyano(hydroxy)phosphinate Chemical compound [Li+].OP([O-])(=O)C#N XYNYNGGQGKVHLU-UHFFFAOYSA-M 0.000 claims description 2
- NXVFZIGLQLFSRM-UHFFFAOYSA-M lithium;cyano(methoxy)phosphinate Chemical compound [Li+].COP([O-])(=O)C#N NXVFZIGLQLFSRM-UHFFFAOYSA-M 0.000 claims description 2
- 229910017604 nitric acid Inorganic materials 0.000 claims description 2
- 229910052763 palladium Inorganic materials 0.000 claims description 2
- 239000010452 phosphate Substances 0.000 claims description 2
- FZGXTGHGJDCOST-UHFFFAOYSA-M potassium;cyano(ethoxy)phosphinate Chemical compound [K+].CCOP([O-])(=O)C#N FZGXTGHGJDCOST-UHFFFAOYSA-M 0.000 claims description 2
- HZUPVLLYKHPYSJ-UHFFFAOYSA-M potassium;cyano(methoxy)phosphinate Chemical compound [K+].COP([O-])(=O)C#N HZUPVLLYKHPYSJ-UHFFFAOYSA-M 0.000 claims description 2
- WRCXDFGMAUJAIF-UHFFFAOYSA-M potassium;hydron;phosphonatoformonitrile Chemical compound [K+].OP([O-])(=O)C#N WRCXDFGMAUJAIF-UHFFFAOYSA-M 0.000 claims description 2
- 229910052703 rhodium Inorganic materials 0.000 claims description 2
- 239000010948 rhodium Substances 0.000 claims description 2
- ZKNMVCPQTZZKLL-UHFFFAOYSA-M sodium;cyano(ethoxy)phosphinate Chemical compound [Na+].CCOP([O-])(=O)C#N ZKNMVCPQTZZKLL-UHFFFAOYSA-M 0.000 claims description 2
- WZPSJNVSRYRJHU-UHFFFAOYSA-M sodium;cyano(hydroxy)phosphinate Chemical compound [Na+].OP([O-])(=O)C#N WZPSJNVSRYRJHU-UHFFFAOYSA-M 0.000 claims description 2
- BWETVQSATXFGKZ-UHFFFAOYSA-M sodium;cyano(methoxy)phosphinate Chemical compound [Na+].COP([O-])(=O)C#N BWETVQSATXFGKZ-UHFFFAOYSA-M 0.000 claims description 2
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 claims description 2
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 claims description 2
- 229920002732 Polyanhydride Polymers 0.000 claims 3
- IAANMKMHMYZVOC-UHFFFAOYSA-N aminomethyl dihydrogen phosphate Chemical compound NCOP(O)(O)=O IAANMKMHMYZVOC-UHFFFAOYSA-N 0.000 claims 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims 1
- 150000005690 diesters Chemical class 0.000 claims 1
- BBEQWMMVPFVUTB-UHFFFAOYSA-L dilithium;phosphonatoformonitrile Chemical compound [Li+].[Li+].[O-]P([O-])(=O)C#N BBEQWMMVPFVUTB-UHFFFAOYSA-L 0.000 claims 1
- QZJYHWXRWTVKSH-UHFFFAOYSA-N ethylaminomethylphosphonic acid Chemical group CCNCP(O)(O)=O QZJYHWXRWTVKSH-UHFFFAOYSA-N 0.000 claims 1
- NRZWQKGABZFFKE-UHFFFAOYSA-N trimethylsulfonium Chemical compound C[S+](C)C NRZWQKGABZFFKE-UHFFFAOYSA-N 0.000 claims 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 239000000047 product Substances 0.000 description 8
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 7
- 230000007062 hydrolysis Effects 0.000 description 7
- 238000006460 hydrolysis reaction Methods 0.000 description 7
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 238000004128 high performance liquid chromatography Methods 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 239000002002 slurry Substances 0.000 description 6
- 150000001768 cations Chemical class 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical group [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- 239000011574 phosphorus Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- WORJRXHJTUTINR-UHFFFAOYSA-N 1,4-dioxane;hydron;chloride Chemical compound Cl.C1COCCO1 WORJRXHJTUTINR-UHFFFAOYSA-N 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- 150000002903 organophosphorus compounds Chemical class 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 230000005588 protonation Effects 0.000 description 3
- MDBVZFGSKMWJFD-UHFFFAOYSA-N OP(O)=O.OP(O)(O)=O Chemical compound OP(O)=O.OP(O)(O)=O MDBVZFGSKMWJFD-UHFFFAOYSA-N 0.000 description 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 2
- 229920000388 Polyphosphate Chemical class 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 125000004185 ester group Chemical group 0.000 description 2
- 239000004009 herbicide Substances 0.000 description 2
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 2
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 2
- 239000001205 polyphosphate Chemical class 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- WHHKOTLKOCHMOC-UHFFFAOYSA-N 2-hydroxyethylazanium;phosphonatoformonitrile Chemical compound [NH3+]CCO.[NH3+]CCO.[O-]P([O-])(=O)C#N WHHKOTLKOCHMOC-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- RHLWWCQWCJNRJQ-UHFFFAOYSA-N CN(C)C(CP(O)(O)=O)(N)N(C)C Chemical compound CN(C)C(CP(O)(O)=O)(N)N(C)C RHLWWCQWCJNRJQ-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- AGINPOJWTDKORT-UHFFFAOYSA-N [H]OP(=O)OC([H])([H])N Chemical class [H]OP(=O)OC([H])([H])N AGINPOJWTDKORT-UHFFFAOYSA-N 0.000 description 1
- UUMLZIUNMPFFNP-UHFFFAOYSA-N [cyano-bis(dimethylamino)methyl]phosphonic acid Chemical compound CN(C)C(C#N)(N(C)C)P(=O)(O)O UUMLZIUNMPFFNP-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 229940058344 antitrematodals organophosphorous compound Drugs 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 230000005595 deprotonation Effects 0.000 description 1
- 238000010537 deprotonation reaction Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- SMBQBQBNOXIFSF-UHFFFAOYSA-N dilithium Chemical compound [Li][Li] SMBQBQBNOXIFSF-UHFFFAOYSA-N 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical class [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- LEUKBEHSJIXCMG-UHFFFAOYSA-M lithium;cyano(phenylmethoxy)phosphinate Chemical compound [Li+].N#CP(=O)([O-])OCC1=CC=CC=C1 LEUKBEHSJIXCMG-UHFFFAOYSA-M 0.000 description 1
- CPGKYVRDHFHPNX-UHFFFAOYSA-M lithium;cyano-(2,6-dichlorophenoxy)phosphinate Chemical compound [Li+].N#CP(=O)([O-])OC1=C(Cl)C=CC=C1Cl CPGKYVRDHFHPNX-UHFFFAOYSA-M 0.000 description 1
- GDISJVJMBKYQMD-UHFFFAOYSA-M lithium;cyano-(4-nitrophenoxy)phosphinate Chemical compound [Li+].[O-][N+](=O)C1=CC=C(OP([O-])(=O)C#N)C=C1 GDISJVJMBKYQMD-UHFFFAOYSA-M 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical class O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 1
- BTRFCOAPCSJHJX-UHFFFAOYSA-L phosphonatoformonitrile;trimethylsulfanium Chemical compound C[S+](C)C.C[S+](C)C.[O-]P([O-])(=O)C#N BTRFCOAPCSJHJX-UHFFFAOYSA-L 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 1
- HCHCMWUUWKHMBC-UHFFFAOYSA-M potassium;cyano(phenylmethoxy)phosphinate Chemical compound [K+].N#CP(=O)([O-])OCC1=CC=CC=C1 HCHCMWUUWKHMBC-UHFFFAOYSA-M 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- HBVYBEQVLAYKDS-UHFFFAOYSA-M sodium;cyano(phenylmethoxy)phosphinate Chemical compound [Na+].N#CP(=O)([O-])OCC1=CC=CC=C1 HBVYBEQVLAYKDS-UHFFFAOYSA-M 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/3804—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
- C07F9/3808—Acyclic saturated acids which can have further substituents on alkyl
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US3451596P | 1996-12-30 | 1996-12-30 | |
| PCT/US1997/023500 WO1998029423A1 (en) | 1996-12-30 | 1997-12-23 | Hydrogenation of cyanophosphonate derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL130705A0 IL130705A0 (en) | 2000-06-01 |
| IL130705A true IL130705A (en) | 2002-11-10 |
Family
ID=21876898
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL13070597A IL130705A (en) | 1996-12-30 | 1997-12-23 | Hydrogenation of cyanophosphate history |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US5905163A (pt) |
| EP (1) | EP0948507A1 (pt) |
| JP (1) | JP2001507695A (pt) |
| AR (1) | AR012833A1 (pt) |
| AU (1) | AU723432B2 (pt) |
| BR (1) | BR9714449A (pt) |
| CA (1) | CA2276187A1 (pt) |
| IL (1) | IL130705A (pt) |
| WO (1) | WO1998029423A1 (pt) |
| ZA (1) | ZA9711675B (pt) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0948326B1 (en) * | 1996-12-30 | 2002-09-18 | Monsanto Technology LLC | Method for preparing cyanophosphonate derivatives from phosphoric anhydride and cyanide |
| US20070099783A1 (en) * | 2005-10-27 | 2007-05-03 | Rennco, Inc. | Bag forming device |
| US7947130B2 (en) | 2009-10-24 | 2011-05-24 | Wai Mun Lee | Troika acid semiconductor cleaning compositions and methods of use |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE300936C (pt) * | ||||
| US2402703A (en) * | 1942-08-06 | 1946-06-25 | Victor Chemical Works | Method of producing neutral esters of molecularly dehydrated phosphoric acids |
| US2702299A (en) * | 1948-05-01 | 1955-02-15 | Monsanto Chemicals | Manufacture of tetraethyl pyrophosphate |
| US3432277A (en) * | 1966-08-03 | 1969-03-11 | Du Pont | Derivatives of phosphinodithionic acid and method for their preparation |
| DE2032712C3 (de) * | 1970-07-02 | 1978-10-19 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von w-Amino-alkanphosphonsäure bzw.- phosphinsäurederivaten |
| JPS5838437B2 (ja) * | 1974-08-20 | 1983-08-23 | ニツポウカガク カブシキガイシヤ | ジアルキルシアノホスホネ−トノ セイゾウホウホウ |
| US4221583A (en) * | 1978-12-22 | 1980-09-09 | Monsanto Company | N-Phosphonomethylglycinonitrile and certain derivatives thereof |
| US4568432A (en) * | 1984-12-28 | 1986-02-04 | Monsanto Company | Process for preparing glyphosate and glyphosate derivatives |
| GB9423254D0 (en) * | 1994-11-16 | 1995-01-04 | Zeneca Ltd | Process |
-
1997
- 1997-12-23 IL IL13070597A patent/IL130705A/en not_active IP Right Cessation
- 1997-12-23 CA CA002276187A patent/CA2276187A1/en not_active Abandoned
- 1997-12-23 EP EP97954790A patent/EP0948507A1/en not_active Withdrawn
- 1997-12-23 JP JP53011498A patent/JP2001507695A/ja active Pending
- 1997-12-23 BR BR9714449A patent/BR9714449A/pt not_active IP Right Cessation
- 1997-12-23 US US08/996,948 patent/US5905163A/en not_active Expired - Fee Related
- 1997-12-23 AU AU60132/98A patent/AU723432B2/en not_active Ceased
- 1997-12-23 WO PCT/US1997/023500 patent/WO1998029423A1/en not_active Application Discontinuation
- 1997-12-29 ZA ZA9711675A patent/ZA9711675B/xx unknown
- 1997-12-30 AR ARP970106293A patent/AR012833A1/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| AU723432B2 (en) | 2000-08-24 |
| AU6013298A (en) | 1998-07-31 |
| WO1998029423A1 (en) | 1998-07-09 |
| IL130705A0 (en) | 2000-06-01 |
| JP2001507695A (ja) | 2001-06-12 |
| EP0948507A1 (en) | 1999-10-13 |
| BR9714449A (pt) | 2000-03-21 |
| ZA9711675B (en) | 1999-06-15 |
| US5905163A (en) | 1999-05-18 |
| AR012833A1 (es) | 2000-11-22 |
| CA2276187A1 (en) | 1998-07-09 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| HK | Corrigendum |
Free format text: JOURNAL NO. 8/02 IN APPLICATION NO. 130705 ON P. 3260, CORRECT THE PRIORITY DATE TO 19961230 |
|
| FF | Patent granted | ||
| RH1 | Patent not in force |