DD264921A5 - Verfahren zur herstellung von n-sulfonyl-acetamido-aminomethan-phosphonaten - Google Patents
Verfahren zur herstellung von n-sulfonyl-acetamido-aminomethan-phosphonaten Download PDFInfo
- Publication number
- DD264921A5 DD264921A5 DD87310642A DD31064287A DD264921A5 DD 264921 A5 DD264921 A5 DD 264921A5 DD 87310642 A DD87310642 A DD 87310642A DD 31064287 A DD31064287 A DD 31064287A DD 264921 A5 DD264921 A5 DD 264921A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- alkyl
- formula
- group
- groups
- carbon atoms
- Prior art date
Links
- -1 N-SULFONYL-ACETAMIDO-AMINOMETHANE Chemical compound 0.000 title description 4
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000006243 chemical reaction Methods 0.000 claims abstract description 9
- 125000005843 halogen group Chemical group 0.000 claims abstract description 6
- 238000002360 preparation method Methods 0.000 claims abstract description 5
- 238000000034 method Methods 0.000 claims description 19
- 125000000217 alkyl group Chemical group 0.000 claims description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 9
- 125000003118 aryl group Chemical group 0.000 claims description 7
- 239000012074 organic phase Substances 0.000 claims description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- 238000004064 recycling Methods 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical compound BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 claims description 3
- 229930195733 hydrocarbon Natural products 0.000 claims description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 2
- 239000004215 Carbon black (E152) Substances 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 229910052740 iodine Inorganic materials 0.000 claims description 2
- 150000002576 ketones Chemical class 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 238000006386 neutralization reaction Methods 0.000 claims description 2
- 150000002825 nitriles Chemical group 0.000 claims description 2
- 239000012429 reaction media Substances 0.000 claims description 2
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims 1
- 125000005599 alkyl carboxylate group Chemical group 0.000 claims 1
- 239000011260 aqueous acid Substances 0.000 claims 1
- 150000008282 halocarbons Chemical class 0.000 claims 1
- 239000003880 polar aprotic solvent Substances 0.000 claims 1
- 238000000926 separation method Methods 0.000 claims 1
- 239000004009 herbicide Substances 0.000 abstract description 2
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 39
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000012071 phase Substances 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
- OJTRKMSUJCHVMW-UHFFFAOYSA-N 2-chloro-n-methyl-n-methylsulfonylacetamide Chemical compound CS(=O)(=O)N(C)C(=O)CCl OJTRKMSUJCHVMW-UHFFFAOYSA-N 0.000 description 4
- VJPHWIBYCFXNDG-UHFFFAOYSA-N P(O)(O)=O.C(C)(C)C(NCC1=CC=CC=C1)C(C)C Chemical compound P(O)(O)=O.C(C)(C)C(NCC1=CC=CC=C1)C(C)C VJPHWIBYCFXNDG-UHFFFAOYSA-N 0.000 description 4
- 239000008346 aqueous phase Substances 0.000 description 4
- 238000004587 chromatography analysis Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 150000003254 radicals Chemical class 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- OYWRDHBGMCXGFY-UHFFFAOYSA-N 1,2,3-triazinane Chemical class C1CNNNC1 OYWRDHBGMCXGFY-UHFFFAOYSA-N 0.000 description 1
- ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical group CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- SAEILGZODTXRSQ-UHFFFAOYSA-N N-[di(propan-2-yloxy)phosphorylmethyl]-1-phenylmethanamine Chemical compound C(C1=CC=CC=C1)NCP(OC(C)C)(=O)OC(C)C SAEILGZODTXRSQ-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- PRLFVZKTUXSRBM-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C.CC=C PRLFVZKTUXSRBM-UHFFFAOYSA-N 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 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)]
- C07F9/44—Amides thereof
-
- 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)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Fertilizers (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Cephalosporin Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8618308A FR2608609B1 (fr) | 1986-12-18 | 1986-12-18 | Preparation d'intermediaires phosphores pour usage herbicide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD264921A5 true DD264921A5 (de) | 1989-02-15 |
Family
ID=9342391
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD87310642A DD264921A5 (de) | 1986-12-18 | 1987-12-17 | Verfahren zur herstellung von n-sulfonyl-acetamido-aminomethan-phosphonaten |
Country Status (18)
| Country | Link |
|---|---|
| EP (1) | EP0275804B1 (pt) |
| JP (1) | JPS63165391A (pt) |
| KR (1) | KR880007408A (pt) |
| CN (1) | CN87105951A (pt) |
| AT (1) | ATE67998T1 (pt) |
| AU (1) | AU599729B2 (pt) |
| BR (1) | BR8706887A (pt) |
| CA (1) | CA1297493C (pt) |
| DD (1) | DD264921A5 (pt) |
| DE (1) | DE3773482D1 (pt) |
| DK (1) | DK665087A (pt) |
| ES (1) | ES2025201B3 (pt) |
| FR (1) | FR2608609B1 (pt) |
| GR (1) | GR3003011T3 (pt) |
| HU (1) | HU202881B (pt) |
| IL (1) | IL84482A (pt) |
| PT (1) | PT86395B (pt) |
| ZA (1) | ZA879478B (pt) |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2575161B1 (fr) * | 1984-12-26 | 1989-03-31 | Rhone Poulenc Agrochimie | Preparation d'intermediaires phosphores pour usages herbicides |
| FR2576024B1 (fr) * | 1985-01-14 | 1988-01-08 | Rhone Poulenc Agrochimie | Herbicides de type n - (phosphonomethylglycyl) sulfonylamines |
| FR2590901B1 (fr) * | 1985-12-04 | 1988-07-29 | Rhone Poulenc Agrochimie | Procede de preparation de n-sulfonyl n-(phosphonomethyl-glycyl) amines utilisables comme herbicides |
-
1986
- 1986-12-18 FR FR8618308A patent/FR2608609B1/fr not_active Expired
-
1987
- 1987-11-16 IL IL84482A patent/IL84482A/xx unknown
- 1987-12-12 KR KR870014226A patent/KR880007408A/ko not_active Application Discontinuation
- 1987-12-16 AU AU82618/87A patent/AU599729B2/en not_active Ceased
- 1987-12-16 CA CA000554483A patent/CA1297493C/en not_active Expired - Lifetime
- 1987-12-17 DD DD87310642A patent/DD264921A5/de not_active IP Right Cessation
- 1987-12-17 BR BR8706887A patent/BR8706887A/pt unknown
- 1987-12-17 JP JP62320034A patent/JPS63165391A/ja active Pending
- 1987-12-17 ES ES87420345T patent/ES2025201B3/es not_active Expired - Lifetime
- 1987-12-17 HU HU875755A patent/HU202881B/hu not_active IP Right Cessation
- 1987-12-17 EP EP87420345A patent/EP0275804B1/fr not_active Expired - Lifetime
- 1987-12-17 PT PT86395A patent/PT86395B/pt not_active IP Right Cessation
- 1987-12-17 ZA ZA879478A patent/ZA879478B/xx unknown
- 1987-12-17 CN CN198787105951A patent/CN87105951A/zh active Pending
- 1987-12-17 AT AT87420345T patent/ATE67998T1/de not_active IP Right Cessation
- 1987-12-17 DK DK665087A patent/DK665087A/da not_active Application Discontinuation
- 1987-12-17 DE DE8787420345T patent/DE3773482D1/de not_active Expired - Fee Related
-
1991
- 1991-10-03 GR GR90401219T patent/GR3003011T3/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU8261887A (en) | 1988-06-23 |
| HU202881B (en) | 1991-04-29 |
| EP0275804A1 (fr) | 1988-07-27 |
| CN87105951A (zh) | 1988-06-29 |
| KR880007408A (ko) | 1988-08-27 |
| DK665087A (da) | 1988-06-19 |
| FR2608609B1 (fr) | 1989-06-02 |
| AU599729B2 (en) | 1990-07-26 |
| JPS63165391A (ja) | 1988-07-08 |
| DE3773482D1 (de) | 1991-11-07 |
| IL84482A (en) | 1992-11-15 |
| HUT48634A (en) | 1989-06-28 |
| ZA879478B (en) | 1988-06-14 |
| ATE67998T1 (de) | 1991-10-15 |
| PT86395B (pt) | 1990-11-20 |
| BR8706887A (pt) | 1988-07-26 |
| PT86395A (fr) | 1988-01-01 |
| DK665087D0 (da) | 1987-12-17 |
| CA1297493C (en) | 1992-03-17 |
| FR2608609A1 (fr) | 1988-06-24 |
| GR3003011T3 (en) | 1993-02-17 |
| EP0275804B1 (fr) | 1991-10-02 |
| IL84482A0 (en) | 1988-04-29 |
| ES2025201B3 (es) | 1992-03-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| ENJ | Ceased due to non-payment of renewal fee |