NL8900280A - Werkwijze voor de bereiding van n-fosfono-methyl-imino-diazijnzuur. - Google Patents
Werkwijze voor de bereiding van n-fosfono-methyl-imino-diazijnzuur. Download PDFInfo
- Publication number
- NL8900280A NL8900280A NL8900280A NL8900280A NL8900280A NL 8900280 A NL8900280 A NL 8900280A NL 8900280 A NL8900280 A NL 8900280A NL 8900280 A NL8900280 A NL 8900280A NL 8900280 A NL8900280 A NL 8900280A
- Authority
- NL
- Netherlands
- Prior art keywords
- imino
- acid
- diacetic acid
- phosphono
- methyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 14
- 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 description 12
- 238000002360 preparation method Methods 0.000 title claims description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 21
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 13
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 12
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- KKHJQZVEUKJURX-UHFFFAOYSA-N 2-(carboxymethylamino)acetic acid;hydrochloride Chemical compound Cl.OC(=O)CNCC(O)=O KKHJQZVEUKJURX-UHFFFAOYSA-N 0.000 claims description 8
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 claims description 8
- 239000007864 aqueous solution Substances 0.000 claims description 7
- 159000000007 calcium salts Chemical class 0.000 claims description 7
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 6
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims description 6
- 239000000920 calcium hydroxide Substances 0.000 claims description 6
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims description 6
- NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical compound OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 claims description 6
- 229910021529 ammonia Inorganic materials 0.000 claims description 5
- 238000003756 stirring Methods 0.000 claims description 4
- HQNNCDJMFMJHDH-UHFFFAOYSA-L calcium;2-(carboxylatomethylamino)acetate Chemical compound [Ca+2].[O-]C(=O)CNCC([O-])=O HQNNCDJMFMJHDH-UHFFFAOYSA-L 0.000 claims description 3
- 238000002955 isolation Methods 0.000 claims description 3
- 238000000746 purification Methods 0.000 claims description 3
- 238000001704 evaporation Methods 0.000 claims description 2
- 230000008020 evaporation Effects 0.000 claims description 2
- 239000011541 reaction mixture Substances 0.000 description 11
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 238000009835 boiling Methods 0.000 description 7
- 239000000047 product Substances 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 238000010992 reflux Methods 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000008098 formaldehyde solution Substances 0.000 description 2
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- RVXJYJRESXKWTN-UHFFFAOYSA-N 2-iminoacetic acid;hydrochloride Chemical compound Cl.OC(=O)C=N RVXJYJRESXKWTN-UHFFFAOYSA-N 0.000 description 1
- 239000005562 Glyphosate Substances 0.000 description 1
- GJORGQDICLQHKQ-UHFFFAOYSA-N OC(CNCC(O)=O)=O.Cl.Cl Chemical compound OC(CNCC(O)=O)=O.Cl.Cl GJORGQDICLQHKQ-UHFFFAOYSA-N 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- TVMUHOAONWHJBV-UHFFFAOYSA-N dehydroglycine Chemical compound OC(=O)C=N TVMUHOAONWHJBV-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 229940097068 glyphosate Drugs 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- YMUIJWOIZMVBQZ-UHFFFAOYSA-M sodium;2-(carboxymethylamino)acetate Chemical compound [Na+].OC(=O)CNCC([O-])=O YMUIJWOIZMVBQZ-UHFFFAOYSA-M 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000007858 starting material 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)]
- C07F9/3804—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
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)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU56288 | 1988-02-08 | ||
| HU88562A HU200780B (en) | 1988-02-08 | 1988-02-08 | Process for producing n-phosphonomethyl iminodiacetic acid from double salt of iminodiacetic acid |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NL8900280A true NL8900280A (nl) | 1989-09-01 |
Family
ID=10950170
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL8900280A NL8900280A (nl) | 1988-02-08 | 1989-02-06 | Werkwijze voor de bereiding van n-fosfono-methyl-imino-diazijnzuur. |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US4931585A (pt) |
| JP (1) | JPH01228996A (pt) |
| CN (1) | CN1035293A (pt) |
| AU (1) | AU607040B2 (pt) |
| BE (1) | BE1002095A5 (pt) |
| BR (1) | BR8900621A (pt) |
| DE (1) | DE3903715A1 (pt) |
| DK (1) | DK39789A (pt) |
| ES (1) | ES2010396A6 (pt) |
| FR (1) | FR2626883B1 (pt) |
| GB (1) | GB2215720B (pt) |
| GR (1) | GR890100070A (pt) |
| HU (1) | HU200780B (pt) |
| IT (1) | IT1229522B (pt) |
| NL (1) | NL8900280A (pt) |
| NZ (1) | NZ227703A (pt) |
| PL (1) | PL277488A1 (pt) |
| PT (1) | PT89578B (pt) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5312972A (en) * | 1992-10-29 | 1994-05-17 | Hampshire Chemical Corp. | Conversion of hydroxymethyl-iminodiacetic acid to phosphonomethyl-iminodiacetic acid |
| US5312973A (en) * | 1993-03-25 | 1994-05-17 | Finchimica S.P.A. | Process for producing n-phosphono-methyl-imino-diacetic acid |
| JP3126033B2 (ja) * | 1995-06-07 | 2001-01-22 | モンサント・カンパニー | N−ホスホノメチルイミノジ酢酸を製造する方法 |
| IES980552A2 (en) | 1998-07-09 | 1999-08-11 | Agritech Chemical Ltd | Improved process for preparing N-phosphonomethyl iminodiacetic acid |
| US6118022A (en) * | 1998-09-08 | 2000-09-12 | Hampshire Chemical Corp. | Synthesis of phosphonomethyliminodiacetic acid with reduced effluent |
| CN104854117B (zh) | 2012-07-17 | 2018-12-25 | 孟山都技术有限责任公司 | 用于合成n-膦酰基甲基亚氨基二乙酸的方法 |
| IN2015DN01079A (pt) | 2012-07-17 | 2015-06-26 | Straitmark Holding Ag | |
| BR112015000993B1 (pt) | 2012-07-17 | 2020-04-28 | Monsanto Technology Llc | método para a síntese de um ácido alfaaminoalquileno fosfônico ou de um éster do mesmo |
| RU2674021C9 (ru) | 2012-07-17 | 2019-01-24 | МОНСАНТО ТЕКНОЛОДЖИ ЭлЭлСи | Способ синтеза n-(фосфонометил)глицина |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2895989A (en) * | 1956-06-22 | 1959-07-21 | Dow Chemical Co | Method for the preparation of iminodiacetic acid |
| US3455675A (en) * | 1968-06-25 | 1969-07-15 | Monsanto Co | Aminophosphonate herbicides |
| HU184168B (en) * | 1979-05-11 | 1984-07-30 | Mta Koezponti Kemiai Kutato In | Process for producing n-bracket-phosphono-methyl-bracket closed-glycine |
| US4724103A (en) * | 1984-02-27 | 1988-02-09 | Monsanto Company | Process for preparing N,N-diacetic acid aminomethylenephosphonic acid |
| US4657705A (en) * | 1985-09-23 | 1987-04-14 | Monsanto Company | Process for the preparation of N-substituted aminomethylphosphonic acids |
-
1988
- 1988-02-08 HU HU88562A patent/HU200780B/hu not_active IP Right Cessation
-
1989
- 1989-01-24 NZ NZ227703A patent/NZ227703A/en unknown
- 1989-01-25 AU AU28798/89A patent/AU607040B2/en not_active Expired - Fee Related
- 1989-01-27 DK DK039789A patent/DK39789A/da not_active Application Discontinuation
- 1989-01-27 GB GB8901806A patent/GB2215720B/en not_active Expired - Fee Related
- 1989-01-31 PL PL27748889A patent/PL277488A1/xx unknown
- 1989-01-31 PT PT89578A patent/PT89578B/pt active IP Right Grant
- 1989-02-01 FR FR898901265A patent/FR2626883B1/fr not_active Expired - Fee Related
- 1989-02-02 US US07/306,032 patent/US4931585A/en not_active Expired - Fee Related
- 1989-02-03 BE BE8900121A patent/BE1002095A5/fr not_active IP Right Cessation
- 1989-02-03 IT IT8919299A patent/IT1229522B/it active
- 1989-02-03 BR BR898900621A patent/BR8900621A/pt unknown
- 1989-02-03 CN CN89100720.2A patent/CN1035293A/zh active Pending
- 1989-02-06 GR GR890100070A patent/GR890100070A/el unknown
- 1989-02-06 NL NL8900280A patent/NL8900280A/nl not_active Application Discontinuation
- 1989-02-07 ES ES8900421A patent/ES2010396A6/es not_active Expired
- 1989-02-07 JP JP1028531A patent/JPH01228996A/ja active Pending
- 1989-02-08 DE DE3903715A patent/DE3903715A1/de not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| PL277488A1 (en) | 1989-10-16 |
| DE3903715A1 (de) | 1989-08-17 |
| AU2879889A (en) | 1989-08-10 |
| GB2215720A (en) | 1989-09-27 |
| FR2626883A1 (fr) | 1989-08-11 |
| GB8901806D0 (en) | 1989-03-15 |
| HU200780B (en) | 1990-08-28 |
| US4931585A (en) | 1990-06-05 |
| HUT49360A (en) | 1989-09-28 |
| FR2626883B1 (fr) | 1991-02-22 |
| IT1229522B (it) | 1991-09-03 |
| IT8919299A0 (it) | 1989-02-03 |
| GR890100070A (el) | 1994-03-31 |
| AU607040B2 (en) | 1991-02-21 |
| DK39789D0 (da) | 1989-01-27 |
| CN1035293A (zh) | 1989-09-06 |
| ES2010396A6 (es) | 1989-11-01 |
| DK39789A (da) | 1989-08-09 |
| GB2215720B (en) | 1991-07-10 |
| BR8900621A (pt) | 1989-10-10 |
| PT89578B (pt) | 1994-01-31 |
| JPH01228996A (ja) | 1989-09-12 |
| BE1002095A5 (fr) | 1990-06-26 |
| NZ227703A (en) | 1990-11-27 |
| PT89578A (pt) | 1989-10-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0027982B1 (de) | Verfahren zur Herstellung von 3-Amino-1-hydroxypropan-1,1-diphosphonsäure | |
| EP0009022B1 (en) | Processes for preparing d,l-2-amino-4((hydroxy)(methyl)phosphinoyl)-butyric acid and an acetal of an ester of 3-oxopropylmethyl phosphinic acid | |
| DE3025657C2 (pt) | ||
| TWI764016B (zh) | 製備o,o-二甲基硫代磷醯酯和n-(甲氧基-甲基呋喃基磷醯基)乙醯胺之方法 | |
| NL8900280A (nl) | Werkwijze voor de bereiding van n-fosfono-methyl-imino-diazijnzuur. | |
| EP1209162B1 (de) | Verfahren zur Herstellung von Aminoalkylsilanen | |
| KR930011283B1 (ko) | 3'-아지도-3'-디옥시디미딘 및 그 유사화합물의 합성방법 | |
| US3036087A (en) | Process for the preparation of phosphocreatine and/or phosphocreatinine | |
| US4272448A (en) | Process for the manufacture of aluminum monoethyl phosphite | |
| CS239903B2 (en) | Processing of aminomethyl phosphoric acid derivatives | |
| EP0026736B1 (de) | Verfahren zur Herstellung von 2,3,5-Trichlorpyridin sowie Ammoniumsalze des Methanphosphonsäuremonomethylesters und deren Herstellung | |
| US4052451A (en) | Preparation of calcium pantothenate | |
| NL8900279A (nl) | Werkwijze voor de bereiding van n-fosfono-methyl-imino-diazijnzuur en zuurchloride. | |
| KR20080007347A (ko) | 오염화인과 디엠에프로부터 부산물로서 옥시염화인의 생성및 빌스마이어-헥크 시약으로의 변환에 의한 염소화 반응에사용되는 옥시염화인의 용도 | |
| NZ262449A (en) | Process for manufacture of aminomethanephosphonic acid and its use to prepare glyphosate | |
| US9896463B2 (en) | Preparation of purified phosphorodiamidite | |
| DE1670114A1 (de) | Penicilline und Verfahren zu ihrer Herstellung | |
| SU545259A3 (ru) | Способ получени -замещенных циклосериновых соединений или их солей | |
| SU376387A1 (ru) | Способ получения фосфорилированных дифениламинов | |
| DE69300691T2 (de) | Verfahren zur Herstellung von Etoposidphosphat und Zwischenprodukte davon. | |
| JPH0692408B2 (ja) | ヒポキサンチン及びその誘導体とグアニン及びその誘導体との相互分離方法 | |
| CA1070305A (en) | Method of producing morpholine compound | |
| DE884367C (de) | Verfahren zur Herstellung von Lactoflavin-monophosphorsaeureestern | |
| SU322884A1 (pt) | ||
| JP2759087B2 (ja) | 1,4―ジヒドロキシ―2―ナフトエ酸アリールエステルの精製方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A1A | A request for search or an international-type search has been filed | ||
| BB | A search report has been drawn up | ||
| BV | The patent application has lapsed |