DD254011A5 - Verfahren zur herstellung von n-sulfonyl-n-(phosphono-methylglycyl)-aminen - Google Patents
Verfahren zur herstellung von n-sulfonyl-n-(phosphono-methylglycyl)-aminen Download PDFInfo
- Publication number
- DD254011A5 DD254011A5 DD86296951A DD29695186A DD254011A5 DD 254011 A5 DD254011 A5 DD 254011A5 DD 86296951 A DD86296951 A DD 86296951A DD 29695186 A DD29695186 A DD 29695186A DD 254011 A5 DD254011 A5 DD 254011A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- formula
- hydrogen atom
- catalyst
- radical
- carbon atoms
- Prior art date
Links
- -1 PHOSPHONO-METHYLGLYCYL Chemical class 0.000 title abstract description 8
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 claims abstract description 14
- 238000002360 preparation method Methods 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract description 16
- 150000001875 compounds Chemical class 0.000 abstract description 11
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 abstract description 7
- 125000003107 substituted aryl group Chemical group 0.000 abstract description 6
- 239000004215 Carbon black (E152) Substances 0.000 abstract description 4
- 229930195733 hydrocarbon Natural products 0.000 abstract description 4
- 230000002363 herbicidal effect Effects 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 description 17
- 125000004432 carbon atom Chemical group C* 0.000 description 15
- 125000000217 alkyl group Chemical group 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 13
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 13
- 150000003839 salts Chemical class 0.000 description 11
- 150000003254 radicals Chemical class 0.000 description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 7
- 239000001257 hydrogen Substances 0.000 description 7
- 238000005984 hydrogenation reaction Methods 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
- 229910052697 platinum Inorganic materials 0.000 description 6
- 125000000753 cycloalkyl group Chemical group 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000004587 chromatography analysis Methods 0.000 description 3
- 239000004009 herbicide Substances 0.000 description 3
- 238000007327 hydrogenolysis reaction Methods 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000005909 Kieselgur Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 2
- 150000003057 platinum Chemical class 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 230000009466 transformation Effects 0.000 description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229910019020 PtO2 Inorganic materials 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- YKIOKAURTKXMSB-UHFFFAOYSA-N adams's catalyst Chemical compound O=[Pt]=O YKIOKAURTKXMSB-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 150000003864 primary ammonium salts Chemical class 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 150000003865 secondary ammonium salts Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 150000003866 tertiary ammonium salts Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8518148A FR2590901B1 (fr) | 1985-12-04 | 1985-12-04 | Procede de preparation de n-sulfonyl n-(phosphonomethyl-glycyl) amines utilisables comme herbicides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD254011A5 true DD254011A5 (de) | 1988-02-10 |
Family
ID=9325549
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD86296951A DD254011A5 (de) | 1985-12-04 | 1986-12-02 | Verfahren zur herstellung von n-sulfonyl-n-(phosphono-methylglycyl)-aminen |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US4868269A (es) |
| JP (1) | JPS63501574A (es) |
| KR (1) | KR880700806A (es) |
| CN (1) | CN86107974A (es) |
| AU (1) | AU6723887A (es) |
| DD (1) | DD254011A5 (es) |
| ES (1) | ES2003956A6 (es) |
| FR (1) | FR2590901B1 (es) |
| IL (1) | IL80858A0 (es) |
| PT (1) | PT83863B (es) |
| WO (1) | WO1987003597A1 (es) |
| ZA (1) | ZA869101B (es) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2608609B1 (fr) * | 1986-12-18 | 1989-06-02 | Rhone Poulenc Agrochimie | Preparation d'intermediaires phosphores pour usage herbicide |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2860342D1 (en) * | 1977-08-11 | 1981-02-12 | Ciba Geigy Ag | Glycylmethyl-phosphinic acid derivatives, their preparation and their use |
| ES8603901A1 (es) * | 1983-07-27 | 1986-01-01 | Rhone Poulenc Agrochimie | Procedimiento de preparacion de sulfonamidas con grupo ansinometilfosfonico |
-
1985
- 1985-12-04 FR FR8518148A patent/FR2590901B1/fr not_active Expired
-
1986
- 1986-11-29 CN CN198686107974A patent/CN86107974A/zh active Pending
- 1986-12-01 AU AU67238/87A patent/AU6723887A/en not_active Abandoned
- 1986-12-01 KR KR870700662A patent/KR880700806A/ko not_active Application Discontinuation
- 1986-12-01 JP JP61506369A patent/JPS63501574A/ja active Pending
- 1986-12-01 WO PCT/FR1986/000410 patent/WO1987003597A1/fr unknown
- 1986-12-02 DD DD86296951A patent/DD254011A5/de unknown
- 1986-12-02 ZA ZA869101A patent/ZA869101B/xx unknown
- 1986-12-03 IL IL80858A patent/IL80858A0/xx unknown
- 1986-12-03 PT PT83863A patent/PT83863B/pt unknown
- 1986-12-03 ES ES8603266A patent/ES2003956A6/es not_active Expired
- 1986-12-04 US US06/937,720 patent/US4868269A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| FR2590901B1 (fr) | 1988-07-29 |
| PT83863B (fr) | 1989-01-03 |
| US4868269A (en) | 1989-09-19 |
| ES2003956A6 (es) | 1988-12-01 |
| PT83863A (fr) | 1987-01-01 |
| CN86107974A (zh) | 1987-07-01 |
| IL80858A0 (en) | 1987-03-31 |
| FR2590901A1 (fr) | 1987-06-05 |
| KR880700806A (ko) | 1988-04-12 |
| WO1987003597A1 (fr) | 1987-06-18 |
| AU6723887A (en) | 1987-06-30 |
| ZA869101B (en) | 1987-07-29 |
| JPS63501574A (ja) | 1988-06-16 |
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