CS195418B1 - Způsob výroby N-fosfonometylglycinu - Google Patents
Způsob výroby N-fosfonometylglycinu Download PDFInfo
- Publication number
- CS195418B1 CS195418B1 CS21676A CS21676A CS195418B1 CS 195418 B1 CS195418 B1 CS 195418B1 CS 21676 A CS21676 A CS 21676A CS 21676 A CS21676 A CS 21676A CS 195418 B1 CS195418 B1 CS 195418B1
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- phosphonomethylglycine
- process according
- diketopiperazine
- bis
- reaction mixture
- Prior art date
Links
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 title claims abstract description 13
- 238000000034 method Methods 0.000 title claims abstract description 12
- 238000009835 boiling Methods 0.000 claims description 8
- 239000011541 reaction mixture Substances 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 6
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 5
- 230000007062 hydrolysis Effects 0.000 claims description 5
- 238000006460 hydrolysis reaction Methods 0.000 claims description 5
- 239000007858 starting material Substances 0.000 claims description 5
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- BXRNXXXXHLBUKK-UHFFFAOYSA-N piperazine-2,5-dione Chemical compound O=C1CNC(=O)CN1 BXRNXXXXHLBUKK-UHFFFAOYSA-N 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- INMIYNYVYZKEMP-UHFFFAOYSA-N (2,3-dioxopiperazin-1-yl)methylphosphonic acid Chemical compound P(=O)(O)(O)CN1C(C(NCC1)=O)=O INMIYNYVYZKEMP-UHFFFAOYSA-N 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- MOFCYHDQWIZKMY-UHFFFAOYSA-N chloromethylphosphonic acid Chemical compound OP(O)(=O)CCl MOFCYHDQWIZKMY-UHFFFAOYSA-N 0.000 description 5
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 4
- -1 phosphonomethyl Chemical group 0.000 description 4
- 241000196324 Embryophyta Species 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- 241000508725 Elymus repens Species 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 2
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 241000245665 Taraxacum Species 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 230000002363 herbicidal effect Effects 0.000 description 2
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 2
- 235000009973 maize Nutrition 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- LYQCDRHQPKKJFN-UHFFFAOYSA-N 1-(chloromethyl)piperazine-2,3-dione Chemical compound ClCN1C(C(NCC1)=O)=O LYQCDRHQPKKJFN-UHFFFAOYSA-N 0.000 description 1
- 244000052363 Cynodon dactylon Species 0.000 description 1
- 241000234653 Cyperus Species 0.000 description 1
- 240000004585 Dactylis glomerata Species 0.000 description 1
- 241000234642 Festuca Species 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical class Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 240000004658 Medicago sativa Species 0.000 description 1
- 235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001348 alkyl chlorides Chemical class 0.000 description 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 125000001475 halogen functional group Chemical group 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 235000011167 hydrochloric acid Nutrition 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical class CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000002420 orchard Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- FIKAKWIAUPDISJ-UHFFFAOYSA-L paraquat dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 FIKAKWIAUPDISJ-UHFFFAOYSA-L 0.000 description 1
- WEYVCQFUGFRXOM-UHFFFAOYSA-N perazine Chemical compound C1CN(C)CCN1CCCN1C2=CC=CC=C2SC2=CC=CC=C21 WEYVCQFUGFRXOM-UHFFFAOYSA-N 0.000 description 1
- 229960002195 perazine Drugs 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HUCI001538 HU170684B (enrdf_load_stackoverflow) | 1975-01-16 | 1975-01-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
CS195418B1 true CS195418B1 (cs) | 1980-02-29 |
Family
ID=10994551
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CS21676A CS195418B1 (cs) | 1975-01-16 | 1976-01-13 | Způsob výroby N-fosfonometylglycinu |
Country Status (3)
Country | Link |
---|---|
CS (1) | CS195418B1 (enrdf_load_stackoverflow) |
HU (1) | HU170684B (enrdf_load_stackoverflow) |
SU (1) | SU589924A3 (enrdf_load_stackoverflow) |
-
1975
- 1975-01-16 HU HUCI001538 patent/HU170684B/hu unknown
-
1976
- 1976-01-13 CS CS21676A patent/CS195418B1/cs unknown
- 1976-01-13 SU SU762311248A patent/SU589924A3/ru active
Also Published As
Publication number | Publication date |
---|---|
SU589924A3 (ru) | 1978-01-25 |
HU170684B (enrdf_load_stackoverflow) | 1977-08-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4065491A (en) | Process for the preparation of N-phosphonomethyl-glycine | |
SU704457A3 (ru) | Способ получени диариловых эфиров -фосфонометилглицинонитрила или их солей | |
EP0098159B1 (en) | Preparation of n-phosphonomethylglycine | |
EP0102694B1 (en) | Method for preparation of n-phosphonomethylglycine | |
US4415503A (en) | Method for preparation of N-phosphonomethylglycine | |
US4427599A (en) | Method for preparation of N-phosphonomethylglycine | |
CA1276174C (en) | Process for the preparation of n-substituted aminomethylphosphonic acids | |
JPH0257077B2 (enrdf_load_stackoverflow) | ||
US5068404A (en) | Thermal dealkylation of N-alkyl N-phosphonomethylglycine | |
JPS5922718B2 (ja) | ビス−n,n′−(ホスホノメチル)−ジケトピペラジン | |
JP3547441B2 (ja) | 製法 | |
CS195418B1 (cs) | Způsob výroby N-fosfonometylglycinu | |
Yavari et al. | An efficient synthesis of stable phosphorus ylides derived from hydantoin and 5, 5-dialkylhydantoins | |
EP0187633B1 (en) | Thermal dealkylation of n-alkyl n-phosphonomethylglycine | |
US4482504A (en) | Method for preparation of N-phosphonomethylglycine | |
US5099056A (en) | Process for the production of n-substituted-aminomethylphosphonic acid dialkylesters and of the corresponding acids | |
US4525311A (en) | O,O-Dialkyl-N-(benzyl or t-butyl)-N-cyanomethyl aminomethylphosphonates | |
RU2674021C2 (ru) | Способ синтеза n-(фосфонометил)глицина | |
US3222378A (en) | Phthalimidomethyl phosphorus compounds | |
JPS6325582B2 (enrdf_load_stackoverflow) | ||
IE912920A1 (en) | Process for the preparation of aminomethylphosphonic acid¹and aminomethylphosphinic acids | |
US4694082A (en) | Compound 1,4-diisopropyl-2,5-diketopiperazine | |
US4569802A (en) | Method for preparation of N-phosphonomethylglycine | |
US4476063A (en) | N-Acylaminomethyl-N-cyanomethyl phosphonates | |
US4351779A (en) | Process for the production of methylaminomethylphosphonic acid esters |