RU2015103314A - Способ синтеза N-фосфонометилиминодиуксусной кислоты - Google Patents
Способ синтеза N-фосфонометилиминодиуксусной кислоты Download PDFInfo
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- RU2015103314A RU2015103314A RU2015103314A RU2015103314A RU2015103314A RU 2015103314 A RU2015103314 A RU 2015103314A RU 2015103314 A RU2015103314 A RU 2015103314A RU 2015103314 A RU2015103314 A RU 2015103314A RU 2015103314 A RU2015103314 A RU 2015103314A
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- Prior art keywords
- acid
- group
- compound
- fragments
- anhydride
- Prior art date
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- 238000000034 method Methods 0.000 title claims abstract 17
- AZIHIQIVLANVKD-UHFFFAOYSA-N N-(phosphonomethyl)iminodiacetic acid Chemical compound OC(=O)CN(CC(O)=O)CP(O)(O)=O AZIHIQIVLANVKD-UHFFFAOYSA-N 0.000 title claims abstract 16
- 230000015572 biosynthetic process Effects 0.000 title claims abstract 5
- 238000003786 synthesis reaction Methods 0.000 title claims abstract 3
- 150000001875 compounds Chemical class 0.000 claims abstract 27
- 229910004856 P—O—P Inorganic materials 0.000 claims abstract 15
- 150000008064 anhydrides Chemical group 0.000 claims abstract 15
- -1 carboxylate esters Chemical class 0.000 claims abstract 12
- 230000003647 oxidation Effects 0.000 claims abstract 8
- 238000007254 oxidation reaction Methods 0.000 claims abstract 8
- 239000003377 acid catalyst Substances 0.000 claims abstract 7
- 125000004437 phosphorous atom Chemical group 0.000 claims abstract 7
- 150000003839 salts Chemical class 0.000 claims abstract 6
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims abstract 4
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims abstract 4
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract 4
- 229910018828 PO3H2 Inorganic materials 0.000 claims abstract 3
- 239000011541 reaction mixture Substances 0.000 claims abstract 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims abstract 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims abstract 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 2
- 239000001257 hydrogen Substances 0.000 claims abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 2
- JJWLVOIRVHMVIS-UHFFFAOYSA-O isopropylaminium Chemical compound CC(C)[NH3+] JJWLVOIRVHMVIS-UHFFFAOYSA-O 0.000 claims abstract 2
- 150000002825 nitriles Chemical class 0.000 claims abstract 2
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims abstract 2
- 239000011591 potassium Substances 0.000 claims abstract 2
- 229910052700 potassium Inorganic materials 0.000 claims abstract 2
- 239000011734 sodium Substances 0.000 claims abstract 2
- 229910052708 sodium Inorganic materials 0.000 claims abstract 2
- NRZWQKGABZFFKE-UHFFFAOYSA-N trimethylsulfonium Chemical compound C[S+](C)C NRZWQKGABZFFKE-UHFFFAOYSA-N 0.000 claims abstract 2
- 239000012634 fragment Substances 0.000 claims 10
- 239000007787 solid Substances 0.000 claims 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims 3
- 239000007848 Bronsted acid Substances 0.000 claims 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims 3
- 239000002841 Lewis acid Substances 0.000 claims 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 3
- 230000007062 hydrolysis Effects 0.000 claims 3
- 238000006460 hydrolysis reaction Methods 0.000 claims 3
- 230000003993 interaction Effects 0.000 claims 3
- 150000007517 lewis acids Chemical class 0.000 claims 3
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 claims 2
- SULGDUIIWNDPRQ-UHFFFAOYSA-N 2-[carboxymethyl(hydroxymethyl)amino]acetic acid Chemical compound OC(=O)CN(CO)CC(O)=O SULGDUIIWNDPRQ-UHFFFAOYSA-N 0.000 claims 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 claims 2
- RDXABLXNTVBVML-UHFFFAOYSA-N diethoxyphosphanyl diethyl phosphite Chemical compound CCOP(OCC)OP(OCC)OCC RDXABLXNTVBVML-UHFFFAOYSA-N 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 claims 2
- 239000000126 substance Substances 0.000 claims 2
- 239000000758 substrate Substances 0.000 claims 2
- VSAISIQCTGDGPU-UHFFFAOYSA-N tetraphosphorus hexaoxide Chemical compound O1P(O2)OP3OP1OP2O3 VSAISIQCTGDGPU-UHFFFAOYSA-N 0.000 claims 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims 2
- ZXMGHDIOOHOAAE-UHFFFAOYSA-N 1,1,1-trifluoro-n-(trifluoromethylsulfonyl)methanesulfonamide Chemical compound FC(F)(F)S(=O)(=O)NS(=O)(=O)C(F)(F)F ZXMGHDIOOHOAAE-UHFFFAOYSA-N 0.000 claims 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims 1
- LOMCDDMWGIBLBP-UHFFFAOYSA-N 2-[bis(2-ethoxy-2-oxoethyl)amino]acetic acid Chemical compound CCOC(=O)CN(CC(O)=O)CC(=O)OCC LOMCDDMWGIBLBP-UHFFFAOYSA-N 0.000 claims 1
- CCXFBLJCVQRDMG-UHFFFAOYSA-N 2-[bis(2-methoxy-2-oxoethyl)amino]acetic acid Chemical compound COC(=O)CN(CC(O)=O)CC(=O)OC CCXFBLJCVQRDMG-UHFFFAOYSA-N 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical group [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
- 229910006069 SO3H Inorganic materials 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 230000002378 acidificating effect Effects 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- MPMBRWOOISTHJV-UHFFFAOYSA-N but-1-enylbenzene Chemical compound CCC=CC1=CC=CC=C1 MPMBRWOOISTHJV-UHFFFAOYSA-N 0.000 claims 1
- 125000002843 carboxylic acid group Chemical group 0.000 claims 1
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 239000003729 cation exchange resin Substances 0.000 claims 1
- 229940023913 cation exchange resins Drugs 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 claims 1
- CZHYKKAKFWLGJO-UHFFFAOYSA-N dimethyl phosphite Chemical compound COP([O-])OC CZHYKKAKFWLGJO-UHFFFAOYSA-N 0.000 claims 1
- 150000004820 halides Chemical group 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 239000002815 homogeneous catalyst Substances 0.000 claims 1
- 238000011081 inoculation Methods 0.000 claims 1
- 229920000592 inorganic polymer Polymers 0.000 claims 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims 1
- 229910044991 metal oxide Inorganic materials 0.000 claims 1
- 150000004706 metal oxides Chemical class 0.000 claims 1
- 229940098779 methanesulfonic acid Drugs 0.000 claims 1
- FMPDVLYBTCFKCB-UHFFFAOYSA-N methyl 2-[hydroxymethyl-(2-methoxy-2-oxoethyl)amino]acetate Chemical compound COC(=O)CN(CO)CC(=O)OC FMPDVLYBTCFKCB-UHFFFAOYSA-N 0.000 claims 1
- 229910052750 molybdenum Chemical group 0.000 claims 1
- 239000011733 molybdenum Chemical group 0.000 claims 1
- 150000007524 organic acids Chemical class 0.000 claims 1
- 229920000620 organic polymer Polymers 0.000 claims 1
- 150000003009 phosphonic acids Chemical class 0.000 claims 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical class OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims 1
- 229910052698 phosphorus Inorganic materials 0.000 claims 1
- 239000011574 phosphorus Substances 0.000 claims 1
- CYJAWBVQRMVFEO-UHFFFAOYSA-N piperazine-2,6-dione Chemical compound O=C1CNCC(=O)N1 CYJAWBVQRMVFEO-UHFFFAOYSA-N 0.000 claims 1
- 239000002243 precursor Substances 0.000 claims 1
- 239000012429 reaction media Substances 0.000 claims 1
- 239000011347 resin Substances 0.000 claims 1
- 229920005989 resin Polymers 0.000 claims 1
- 229910052710 silicon Inorganic materials 0.000 claims 1
- 239000010703 silicon Substances 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 claims 1
- 125000000542 sulfonic acid group Chemical group 0.000 claims 1
- 150000003460 sulfonic acids Chemical class 0.000 claims 1
- 238000003419 tautomerization reaction Methods 0.000 claims 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 claims 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical group [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims 1
- 229910052721 tungsten Inorganic materials 0.000 claims 1
- 239000010937 tungsten Substances 0.000 claims 1
- 125000005599 alkyl carboxylate group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- OBSZRRSYVTXPNB-UHFFFAOYSA-N tetraphosphorus Chemical compound P12P3P1P32 OBSZRRSYVTXPNB-UHFFFAOYSA-N 0.000 abstract 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)]
- C07F9/3804—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
- C07F9/3813—N-Phosphonomethylglycine; Salts or complexes thereof
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)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12176749.5 | 2012-07-17 | ||
| EP12176749 | 2012-07-17 | ||
| PCT/EP2013/065119 WO2014012986A1 (en) | 2012-07-17 | 2013-07-17 | Method for the synthesis of n-phosphonomethyliminodiacetic acid |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU2015103314A true RU2015103314A (ru) | 2016-09-10 |
Family
ID=49162114
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2015103314A RU2015103314A (ru) | 2012-07-17 | 2013-07-17 | Способ синтеза N-фосфонометилиминодиуксусной кислоты |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US10364262B2 (enExample) |
| EP (1) | EP2875038A1 (enExample) |
| CN (1) | CN104854117B (enExample) |
| BR (1) | BR112015000988A2 (enExample) |
| IN (1) | IN2015DN01082A (enExample) |
| RU (1) | RU2015103314A (enExample) |
| WO (1) | WO2014012986A1 (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2674021C9 (ru) | 2012-07-17 | 2019-01-24 | МОНСАНТО ТЕКНОЛОДЖИ ЭлЭлСи | Способ синтеза n-(фосфонометил)глицина |
| EP2875038A1 (en) | 2012-07-17 | 2015-05-27 | Straitmark Holding AG | Method for the synthesis of n-phosphonomethyliminodiacetic acid |
| RU2694047C2 (ru) | 2012-07-17 | 2019-07-09 | МОНСАНТО ТЕКНОЛОДЖИ ЭлЭлСи | Способ синтеза аминоалкиленфосфоновой кислоты |
| IN2015DN01081A (enExample) * | 2012-07-17 | 2015-06-26 | Straitmark Holding Ag | |
| CN113816994B (zh) * | 2021-04-01 | 2022-05-27 | 南开大学 | (1,1-二氰基-4-氧)-己基-3-氧化吲哚亚膦酸二乙酯及其衍生物的合成方法 |
| CA3256705A1 (en) * | 2022-06-08 | 2023-12-14 | Academia Sinica | LIPIDS, THE NANOPARTICLES COMPRISING THEM, AND THEIR USES |
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| GB1230121A (enExample) | 1967-01-27 | 1971-04-28 | ||
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| DE2017974A1 (de) | 1970-04-15 | 1971-11-04 | Joh. A. Benckiser Gmbh Chemische Fabrik, 6700 Ludwigshafen | Verfahren zur Herstellung von Aminoalkylenphosphonsäuren |
| US3799758A (en) | 1971-08-09 | 1974-03-26 | Monsanto Co | N-phosphonomethyl-glycine phytotoxicant compositions |
| US3969398A (en) | 1974-05-01 | 1976-07-13 | Monsanto Company | Process for producing N-phosphonomethyl glycine |
| HU173170B (hu) | 1974-06-27 | 1979-03-28 | Chinoin Gyogyszer Es Vegyeszet | Sposob poluchenija n-fosfonometil-glicina |
| US3927080A (en) | 1974-09-03 | 1975-12-16 | Monsanto Co | Process for producing N-phosphonomethyl glycine |
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| CH647528A5 (fr) * | 1978-10-27 | 1985-01-31 | Bcap Biolog Chem Act Pat | Procede pour la preparation de n-phosphonomethylglycine. |
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| JPS5775990A (en) | 1980-10-27 | 1982-05-12 | Mitsubishi Gas Chem Co Inc | Preparation of n,n,n',n'-tetra(phosphonomethyl) diaminoalkane |
| IL66824A0 (en) * | 1982-06-25 | 1982-12-31 | Geshuri Lab Ltd | Process for producing n-phosphonomethylglycine derivatives and herbicidal compounds and compositions prepared thereby |
| US4422982A (en) | 1982-06-30 | 1983-12-27 | Stauffer Chemical Company | Method for preparation of N-phosphonomethylglycine |
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| US4617415A (en) | 1983-12-02 | 1986-10-14 | Monsanto Company | α-Substituted N-phosphonomethyliminodiacetic acid |
| US4654429A (en) | 1983-12-02 | 1987-03-31 | Monsanto Company | Process for the preparation of a glyphosate product |
| GB2154588B (en) | 1984-02-20 | 1987-10-07 | Sunlead Chemical Industry Co L | A process for preparation of n-phosphonomethyl glycine |
| US4724103A (en) | 1984-02-27 | 1988-02-09 | Monsanto Company | Process for preparing N,N-diacetic acid aminomethylenephosphonic acid |
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| HU205944B (en) | 1988-02-08 | 1992-07-28 | Nitrokemia Ipartelepek | Process for producing n-phosphono-methyl-imino-diacetic acid |
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| RO101476A2 (ro) | 1988-08-11 | 1991-12-09 | Intreprinderea Textila, Timisoara, Judetul Timis, Ro | Procedeu de obtinere a unor dialchil n,n-bis-(2-hidroxietil)-aminometilfosfonati |
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| CA2339839A1 (en) | 1998-08-12 | 2000-02-24 | Monsanto Company | Continuous process for the preparation of n-(phosphonomethyl) iminodiacetic acid |
| BR9907000A (pt) | 1998-09-08 | 2000-09-26 | Hampshire Chemical Corp | Sìntese de ácido fosfonometiliminodiacético com efluente reduzido |
| DE19909200C1 (de) | 1999-03-03 | 2000-03-09 | Sueddeutsche Kalkstickstoff | Verfahren zur Herstellung von N-Phosphonomethyliminodiessigsäure |
| DE19914375A1 (de) | 1999-03-30 | 2000-10-05 | Sueddeutsche Kalkstickstoff | Verfahren zur Herstellung von N-Phosphonomethyliminodiessigsäure |
| JP3655135B2 (ja) | 1999-08-23 | 2005-06-02 | 株式会社東芝 | スイッチ装置 |
| DE10019879A1 (de) | 2000-04-20 | 2001-10-25 | Degussa | Verfahren zur Herstellung von 2,5-Diketopiperazinen, neue 2,5-Diketopiperazine und deren Verwendung |
| AU2001275182A1 (en) | 2000-06-01 | 2001-12-11 | Monsanto Technology Llc | Metal-catalysed carboxymethylation in the presence of a promoter |
| EP1353930B1 (de) | 2001-01-12 | 2004-08-11 | Basf Aktiengesellschaft | Verfahren zur herstellung von n-phosphonomethyliminodiessigsäure |
| CN1285600C (zh) | 2004-11-25 | 2006-11-22 | 浙江新安化工集团股份有限公司 | 一种草甘膦制剂及其制备方法 |
| EP1681295A1 (en) | 2005-01-17 | 2006-07-19 | Solutia Europe N.V./S.A. | Process for the manufacture of aminoakylenephosphonic acid compounds in the presence of a heterogeneous catalyst |
| EP1681294A1 (en) | 2005-01-17 | 2006-07-19 | Solutia Europe N.V./S.A. | Process for the manufacture of aminopolyalkylene-phosphonic acid compounds |
| US7799571B2 (en) | 2005-04-01 | 2010-09-21 | Monsanto Technology Llc | Control of N-(phosphonomethyl)iminodiacetic acid conversion in manufacture of glyphosate |
| JP2007022956A (ja) | 2005-07-15 | 2007-02-01 | Mitsubishi Gas Chem Co Inc | 高純度アミノメチレンホスホン酸の製造方法 |
| CL2008003539A1 (es) | 2007-11-28 | 2009-07-03 | Procedimiento para la produccion de p4o6 que comprende mezclar o2 o una mezcla de o2 mas un gas inerte y fosforo en donde el producto obtenido se mantiene dentro de una unidad de reaccion a una temperatura entre los 1600 y 2000 k durante por lo menos 1 segundo. | |
| PL2297169T3 (pl) * | 2008-04-25 | 2015-06-30 | Monsanto Technology Llc | Sposób wytwarzania kwasu aminoalkilenofosfonowego |
| EP2112156A1 (en) | 2008-04-25 | 2009-10-28 | Thermphos International B.V. | Method for the Manufacture of Aminoalkylene Phosphonic Acid |
| US8551437B2 (en) | 2008-11-12 | 2013-10-08 | Straitmark Holding Ag | Process for the manufacture of P4O6 with improved yield |
| US20120130120A1 (en) | 2009-05-28 | 2012-05-24 | Straitmark Holding Ag | Method for the manufacture of phosphonoalkyl iminodiacetic acids |
| CA2775004A1 (en) * | 2009-10-02 | 2011-04-07 | Straitmark Holding Ag | Method for the manufacture of aminohydroxy diphosphonic acids |
| WO2011051309A1 (en) | 2009-10-27 | 2011-05-05 | Straitmark Holding Ag | Method for the manufacture of phosphonoalkyl iminodiacetic acid |
| RU2621444C2 (ru) | 2012-06-13 | 2017-06-06 | Конинклейке Филипс Н.В. | Определение скорости распространения поверхностной волны |
| RU2674023C9 (ru) | 2012-07-17 | 2019-01-24 | МОНСАНТО ТЕКНОЛОДЖИ ЭлЭлСи | Способ синтеза n-(фосфонометил)глицина |
| IN2015DN01081A (enExample) * | 2012-07-17 | 2015-06-26 | Straitmark Holding Ag | |
| EP2875038A1 (en) | 2012-07-17 | 2015-05-27 | Straitmark Holding AG | Method for the synthesis of n-phosphonomethyliminodiacetic acid |
-
2013
- 2013-07-17 EP EP13759988.2A patent/EP2875038A1/en not_active Withdrawn
- 2013-07-17 US US14/415,684 patent/US10364262B2/en active Active
- 2013-07-17 WO PCT/EP2013/065119 patent/WO2014012986A1/en not_active Ceased
- 2013-07-17 IN IN1082DEN2015 patent/IN2015DN01082A/en unknown
- 2013-07-17 BR BR112015000988A patent/BR112015000988A2/pt not_active Application Discontinuation
- 2013-07-17 RU RU2015103314A patent/RU2015103314A/ru not_active Application Discontinuation
- 2013-07-17 CN CN201380037544.9A patent/CN104854117B/zh active Active
Also Published As
| Publication number | Publication date |
|---|---|
| CN104854117A (zh) | 2015-08-19 |
| US10364262B2 (en) | 2019-07-30 |
| IN2015DN01082A (enExample) | 2015-06-26 |
| BR112015000988A2 (pt) | 2017-06-27 |
| EP2875038A1 (en) | 2015-05-27 |
| US20150166584A1 (en) | 2015-06-18 |
| CN104854117B (zh) | 2018-12-25 |
| WO2014012986A1 (en) | 2014-01-23 |
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