KR840009313A - N-포스포노메틸글리신산의 제조방법 - Google Patents

N-포스포노메틸글리신산의 제조방법 Download PDF

Info

Publication number
KR840009313A
KR840009313A KR1019840002652A KR840002652A KR840009313A KR 840009313 A KR840009313 A KR 840009313A KR 1019840002652 A KR1019840002652 A KR 1019840002652A KR 840002652 A KR840002652 A KR 840002652A KR 840009313 A KR840009313 A KR 840009313A
Authority
KR
South Korea
Prior art keywords
acid
salt
iminourea
npmg
phosphonomethylglycine
Prior art date
Application number
KR1019840002652A
Other languages
English (en)
Inventor
베켈 이자크
Original Assignee
벤-지온 게슈리
게슈리 라보러터리즈 리미티드
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 벤-지온 게슈리, 게슈리 라보러터리즈 리미티드 filed Critical 벤-지온 게슈리
Publication of KR840009313A publication Critical patent/KR840009313A/ko

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/38Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
    • C07F9/44Amides thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/38Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
    • C07F9/3804Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
    • C07F9/3808Acyclic saturated acids which can have further substituents on alkyl
    • C07F9/3813N-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)
  • Saccharide Compounds (AREA)

Abstract

내용 없음

Description

N-포스포노메틸글리신산의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (12)

  1. (a)하기 일반 구조식(I)의 N-(포스포노메틸)이미노디아세트산(NPMIDA) 유도체를 산화하여 이미노우레이-강산염을 선택적으로 첨가하므로서 NPMG의 상응하는 이미노우레아염을 생성한 다음:
    상기에서 n은 1또는 2이고, R5,R5',R6및 R6'는 각각 H,NH2,수소 또는 수산기에 의해 선택적으로 치환된 아릴, 싸이클로알킬 또는 직쇄 혹은 측쇄 알킬 또는 알케닐기, 또는 알킬아릴기임(단, R5,R5',R6,R6'중 적어도 하나는 수소임)
    (b)상기염을 NPMG 보다 더 강한 산과 반응시켜 용액중에는 상기 강산의 이미노우레아 염이 남아있게 하는 단계로 구성되어 있는 것을 특징으로 하는 N-포스포노메틸글리신산(NPMG)의 제조방법.
  2. 제1항에 있어서, 이미노우레아 강산염을 산화하기전에 일반 구조식(I)을 갖는 NPMIDA 유도체의 용액에 첨가하는 것을 특징으로 하는 방법.
  3. 제2항에 있어서, 상기 강산이 염산 및 황산으로부터 선택되는 무기산인 것을 특징으로 하는 방법.
  4. 제1항에 있어서, 단계(a)에서 사용하기 위해 상기에서 형성된 강산의 이미노우레아염을 NPMIDA알칼리 금속염과 반응시켜 구조식(I)의 염을 제조하는 재순환 단계(C)를 포함하는 것을 특징으로 하는 방법.
  5. 제1항에 있어서, 산이 염산 및 황산으로부터 선택되는 무기산인 것을 특징으로 하는 N-포스포노메틸글리신산(NPMG)의 제조방법.
  6. 제1항에 있어서, 구조식(I)을 갖는 상기 염을 이미노우레아가 구아니딘, 아미노구아니딘, 디 페닐구아니딘 및 디 -0-돌일 구아니딘으로부터 선택되는 특징으로 하는 N-포스포노메틸글리신산(NPMG)의 제조방법
  7. 제6항에 있어서, 상기 이미노우레아가 구아니딘인 것을 특징으로 하는 N-포스포노메틸글리신산(NPMG)의 제조방법.
  8. 제6힝에 있어서, 상기 이미노우레아가 아미노구 아니딘인 것을 특징으로 하는 N-포스포노메틸글신산(NPMG)의 제조방법.
  9. 제4항에 있어서, 상기 알카리 금속이 나트륨 및 칼륨으로부터 선택되는 것을 특징으로 하는 N-포스포노메틸글리신산(NPMG)의 제조방법.
  10. 제1항에 있어서, 상기 아릴기가 1이상의 할로겐 또는 알킬기에 의해 선택적으로 치환된 페닐인 것을 특징으로 하는 N-포스포노메틸글리신산(NPMG)의 제조방법.
  11. 제1항에 있어서, 상기 산화반응이 약 70℃ 내지 120℃ 에서 신시되는 것을 특징으로 하는 N-포스포노메틸글리신산(NPMG)의 제조방법.
  12. 제1항에 있어서, 상기 산화반응이 금속 또는 활성탄소 촉매존재하에 산소분자-함유가스를 이용하여 실시되는 것을 특징으로 하는 N-포스포노메틸글리신산(NPMG)의 제조방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019840002652A 1983-05-17 1984-05-16 N-포스포노메틸글리신산의 제조방법 KR840009313A (ko)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IL68716A IL68716A (en) 1983-05-17 1983-05-17 Process for producing n-phosphonomethylglycine
IL68716 1983-05-17

Publications (1)

Publication Number Publication Date
KR840009313A true KR840009313A (ko) 1984-12-26

Family

ID=11054267

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019840002652A KR840009313A (ko) 1983-05-17 1984-05-16 N-포스포노메틸글리신산의 제조방법

Country Status (18)

Country Link
US (1) US4507250A (ko)
EP (1) EP0125363A1 (ko)
JP (1) JPS59219298A (ko)
KR (1) KR840009313A (ko)
AU (1) AU559641B2 (ko)
BR (1) BR8402458A (ko)
CS (1) CS244136B2 (ko)
DK (1) DK225184A (ko)
ES (1) ES532472A0 (ko)
FI (1) FI841813A (ko)
GR (1) GR79865B (ko)
HU (1) HUT34758A (ko)
IL (1) IL68716A (ko)
MX (1) MX158086A (ko)
NO (1) NO841910L (ko)
PL (1) PL247721A1 (ko)
PT (1) PT78589B (ko)
ZA (1) ZA843503B (ko)

Families Citing this family (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4582650A (en) * 1985-02-11 1986-04-15 Monsanto Company Oxidation with encapsulated co-catalyst
US4579689A (en) * 1985-02-11 1986-04-01 Monsanto Company Oxidation with coated catalyst
US4696772A (en) * 1985-02-28 1987-09-29 Monsanto Company Amine oxidation using carbon catalyst having oxides removed from surface
US5580841A (en) * 1985-05-29 1996-12-03 Zeneca Limited Solid, phytoactive compositions and method for their preparation
US5468718A (en) * 1985-10-21 1995-11-21 Ici Americas Inc. Liquid, phytoactive compositions and method for their preparation
US5047079A (en) * 1986-08-18 1991-09-10 Ici Americas Inc. Method of preparation and use of solid, phytoactive compositions
US4853159A (en) * 1987-10-26 1989-08-01 Monsanto Company Process for producing N-phosphonomethylglycine
NZ231897A (en) * 1988-12-30 1992-09-25 Monsanto Co Dry water-soluble granular composition comprising glyphosate and a liquid surfactant
US5023369A (en) * 1990-06-25 1991-06-11 Monsanto Company Process for producing N-phosphonomethylglycine
IL101539A (en) 1991-04-16 1998-09-24 Monsanto Europe Sa Mono-ammonium salts of the history of N phosphonomethyl glycyl which are not hygroscopes, their preparations and pesticides containing
DE19500121A1 (de) * 1995-01-04 1996-07-11 Bayer Ag Verfahren zur Herstellung von N-Phosphonomethylglycin
UA66365C2 (en) * 1997-07-22 2004-05-17 Mixtures containing ammonium-glyphosate in high concentration
AU746589B2 (en) * 1997-07-30 2002-05-02 Monsanto Company Process and compositions promoting biological effectiveness of exogenous chemical substances in plants
ITTO980048A1 (it) * 1998-01-20 1999-07-20 Ipici Spa Composizioni erbicide, procedimenti per la loro preparazione ed impieghi
EP1062221B1 (en) * 1998-02-12 2006-05-10 Monsanto Technology LLC Process for making glyphosate by oxidizing n-substituted glyphosates
US6232494B1 (en) 1998-02-12 2001-05-15 Monsanto Company Process for the preparation of N-(phosphonomethyl)glycine by oxidizing N-substituted N-(phosphonomethyl)glycine
JP4669608B2 (ja) * 1998-02-13 2011-04-13 モンサント テクノロジー エルエルシー 外因性化学物質およびシロキサン界面活性剤を含有する貯蔵安定性組成物
US6417133B1 (en) 1998-02-25 2002-07-09 Monsanto Technology Llc Deeply reduced oxidation catalyst and its use for catalyzing liquid phase oxidation reactions
GB9819693D0 (en) 1998-09-10 1998-11-04 Zeneca Ltd Glyphosate formulation
IL143273A0 (en) 1998-11-23 2002-04-21 Monsanto Co Compact storage and shipping system for glyphosate herbicide
HU229572B1 (en) 1998-11-23 2014-02-28 Monsanto Technology Llc Highly concentrated aqueous glyphosate compositions
EP1135024B1 (en) 1998-11-30 2004-12-29 Flamel Technologies Promoting biological effectiveness of exogenous chemical substances in plants
US6369001B1 (en) 1999-08-11 2002-04-09 Monsanto Technology, Llc Microemulsion coformulation of a graminicide and a water-soluble herbicide
US6746976B1 (en) 1999-09-24 2004-06-08 The Procter & Gamble Company Thin until wet structures for acquiring aqueous fluids
JP5433120B2 (ja) 1999-09-30 2014-03-05 モンサント テクノロジー エルエルシー 向上した安定性を有するパッケージミックス農薬組成物
MY158895A (en) * 2000-05-19 2016-11-30 Monsanto Technology Llc Potassium glyphosate formulations
US7135437B2 (en) 2000-05-19 2006-11-14 Monsanto Technology Llc Stable liquid pesticide compositions
US6992045B2 (en) 2000-05-19 2006-01-31 Monsanto Technology Llc Pesticide compositions containing oxalic acid
TWI247746B (en) * 2000-05-22 2006-01-21 Monsanto Co Reaction systems for making N-(phosphonomethyl)glycine compounds
US6300323B1 (en) 2000-08-08 2001-10-09 Ishihara Sangyo Kaisha, Ltd. (Poly)ethereal ammonium salts of herbicides bearing acidic moieties and their use as herbicides
US6921834B2 (en) 2002-05-22 2005-07-26 Dow Agrosciences Llc Continuous process for preparing N-phosphonomethyl glycine
US20050037924A1 (en) * 2002-08-31 2005-02-17 Monsanto Technology Llc Sodium glyphosate compositions and process for their preparation
CN100531573C (zh) * 2002-08-31 2009-08-26 孟山都技术公司 含有二羧酸组分的干燥农药组合物的制备方法
AR037559A1 (es) * 2002-11-19 2004-11-17 Atanor S A Una formulacion herbicida solida de n-fosfonometilglicina, bajo la forma de polvo, granulos o escamas, soluble o dispersable en agua, y el procedimiento para preparar dicha composicion
US8703639B2 (en) * 2004-09-15 2014-04-22 Monsanto Technology Llc Oxidation catalyst and its use for catalyzing liquid phase oxidation reactions
US7223718B2 (en) * 2005-03-07 2007-05-29 Falcon Lab Llc Enhanced glyphosate herbicidal concentrates
US20070049498A1 (en) * 2005-09-01 2007-03-01 Brigance Mickey R Agricultural compositions which enhance performance of herbicides
US8252953B2 (en) 2008-05-01 2012-08-28 Monsanto Technology Llc Metal utilization in supported, metal-containing catalysts
PL2306819T3 (pl) * 2008-06-18 2016-08-31 Stepan Co Koncentrat o ultrawysokim stężeniu glifosatu
PL2337452T3 (pl) 2008-07-03 2015-05-29 Monsanto Technology Llc Połączenia derywatyzowanych sacharydowych środków powierzchniowo czynnych i środków powierzchniowo czynnych stanowiących tlenek eteroaminy jako adiuwanty do herbicydów
US20100113274A1 (en) * 2008-09-29 2010-05-06 Monsanto Technology Llc Glyphosate formulations containing amidoalkylamine surfactants
WO2011008453A2 (en) 2009-06-30 2011-01-20 Monsanto Technology Llc N-phosphonomethylglycine guanidine derivative salts
US20110071027A1 (en) * 2009-09-18 2011-03-24 Volker Heide High strength aqueous glyphosate salt concentrates and methods
JP5529831B2 (ja) * 2010-12-22 2014-06-25 ダウ グローバル テクノロジーズ エルエルシー グリホサート化合物とipbcとの相乗的組み合わせ
US11452289B2 (en) 2016-05-11 2022-09-27 Monsanto Technology Llc Glyphosate formulations containing amidoalkylamine surfactants
EP3628160A1 (en) 2018-09-25 2020-04-01 KWS SAAT SE & Co. KGaA Use of glyphosate herbicide for controlling unwanted vegetation in beta vulgaris growing areas
EP3628738A1 (en) 2018-09-25 2020-04-01 KWS SAAT SE & Co. KGaA Method for controlling weed beets and other weeds

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3954848A (en) * 1972-05-31 1976-05-04 Monsanto Company Process for producing N-phosphonomethyl glycine
US3950402A (en) * 1972-05-31 1976-04-13 Monsanto Company Process for producing N-phosphonomethyl glycine
US3969398A (en) * 1974-05-01 1976-07-13 Monsanto Company Process for producing N-phosphonomethyl glycine
US3907652A (en) * 1974-10-30 1975-09-23 Monsanto Co Electrooxidation of phosphonomethyl amines
ES465139A1 (es) * 1976-12-20 1978-10-01 Monsanto Co Un procedimiento para preparar una mono-o disal de n-fosfo- nometilglicina.
HU184168B (en) * 1979-05-11 1984-07-30 Mta Koezponti Kemiai Kutato In Process for producing n-bracket-phosphono-methyl-bracket closed-glycine
IL65187A (en) * 1982-03-08 1985-03-31 Geshuri Lab Ltd N-phosphonomethylglycine derivatives,processes for their preparation and herbicidal compositions containing them
IL66824A0 (en) * 1982-06-25 1982-12-31 Geshuri Lab Ltd Process for producing n-phosphonomethylglycine derivatives and herbicidal compounds and compositions prepared thereby

Also Published As

Publication number Publication date
DK225184A (da) 1984-11-18
ES8507320A1 (es) 1985-10-01
PT78589A (en) 1984-06-01
GR79865B (ko) 1984-10-31
PL247721A1 (en) 1985-03-26
IL68716A0 (en) 1983-09-30
ZA843503B (en) 1985-02-27
PT78589B (en) 1986-06-26
CS350984A2 (en) 1985-08-15
EP0125363A1 (en) 1984-11-21
AU559641B2 (en) 1987-03-19
BR8402458A (pt) 1985-04-02
JPS59219298A (ja) 1984-12-10
HUT34758A (en) 1985-04-28
NO841910L (no) 1984-11-19
ES532472A0 (es) 1985-10-01
FI841813A (fi) 1984-11-18
MX158086A (es) 1989-01-06
CS244136B2 (en) 1986-07-17
IL68716A (en) 1987-03-31
US4507250A (en) 1985-03-26
FI841813A0 (fi) 1984-05-07
DK225184D0 (da) 1984-05-07
AU2781884A (en) 1984-11-22

Similar Documents

Publication Publication Date Title
KR840009313A (ko) N-포스포노메틸글리신산의 제조방법
KR840004437A (ko) 설타미실린의 결정형 벤젠설포네이트 염의 제조방법
DE59808194D1 (de) Verfahren zur herstellung von triazolinthion-derivaten
KR840006333A (ko) 아미노알킬술폰산류의 제조법
KR850001224A (ko) 아미노 메틸 포스폰기를 함유하는 술폰이미드계 제초제의 제조방법
KR840005155A (ko) N-포스포노메틸글리신의 제조방법
KR910006214A (ko) α-히드록시카르복시산 아미드의 제조방법
TW460445B (en) A process for the preparation of methanesulfonic acid
KR850001724A (ko) 4-페닐-4-옥소-부텐-2-오인산유도체의 제조방법
KR920006321A (ko) 3-메틸피라졸의 제조방법
KR860002524A (ko) 신규백금착체의 제조방법
KR860004035A (ko) N-아릴 트리아졸의 제조방법
KR830006196A (ko) 2-메르캅토에틸아민 할로겐화수소산 염류의 제조방법
KR830005191A (ko) 푸란유도체의 제조방법
KR950008490A (ko) 히드록시옥사알킬멜라민류의 제조방법
KR940701401A (ko) N- 포스포노메틸글리신의 유기염 제조방법
KR840005813A (ko) 5,8-디하이드로-8-옥소-1,3-디옥솔로(4,5-g)퀴놀린-7-카복실산류의 제조방법
KR840004081A (ko) 설포닐 우레아의 제조방법
DE3682816D1 (de) Verfahren zur herstellung von 2-carboxypyrazin-4-oxiden.
KR840009301A (ko) 2-퀴녹살리놀의 제조방법
KR870001174A (ko) 2-시아노아미노-피리미딘 유도체의 제조방법
KR970701180A (ko) 3-이속사졸카복실산의 제조 방법(process for producing 3-isoxazole-carboxylic acid)
KR850000387A (ko) 시아노히드린의 제조방법
KR890014504A (ko) 4-(2'-시아노 에틸티오)메틸-2-구아니디노티아졸의 제조방법
KR870010066A (ko) α- 아미노 알킬 포스폰산의 제조방법

Legal Events

Date Code Title Description
WITN Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid