AR124965A1 - Un proceso para la producción de acefato - Google Patents

Un proceso para la producción de acefato

Info

Publication number
AR124965A1
AR124965A1 ARP220100402A ARP220100402A AR124965A1 AR 124965 A1 AR124965 A1 AR 124965A1 AR P220100402 A ARP220100402 A AR P220100402A AR P220100402 A ARP220100402 A AR P220100402A AR 124965 A1 AR124965 A1 AR 124965A1
Authority
AR
Argentina
Prior art keywords
dimethyl
acephate
methamidophos
contacting
process according
Prior art date
Application number
ARP220100402A
Other languages
English (en)
Inventor
Atul Wankhade
Pathik Shah
Praful Sonawane
Amul Desai
Original Assignee
Upl Ltd
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 Upl Ltd filed Critical Upl Ltd
Publication of AR124965A1 publication Critical patent/AR124965A1/es

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
    • C07F9/06Phosphorus compounds without P—C bonds
    • C07F9/22Amides of acids of phosphorus
    • C07F9/24Esteramides
    • C07F9/2454Esteramides the amide moiety containing a substituent or a structure which is considered as characteristic
    • C07F9/2479Compounds containing the structure P(=X)n-N-acyl, P(=X)n-N-heteroatom, P(=X)n-N-CN (X = O, S, Se; n = 0, 1)
    • C07F9/2487Compounds containing the structure P(=X)n-N-acyl, P(=X)n-N-heteroatom, P(=X)n-N-CN (X = O, S, Se; n = 0, 1) containing the structure P(=X)n-N-C(=X) (X = O, S, Se; n = 0, 1)
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/0093Microreactors, e.g. miniaturised or microfabricated reactors
    • 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
    • C07F9/06Phosphorus compounds without P—C bonds
    • C07F9/22Amides of acids of phosphorus
    • C07F9/24Esteramides
    • C07F9/2404Esteramides the ester moiety containing a substituent or a structure which is considered as characteristic
    • C07F9/2408Esteramides the ester moiety containing a substituent or a structure which is considered as characteristic of hydroxyalkyl compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00002Chemical plants
    • B01J2219/00027Process aspects
    • B01J2219/00033Continuous processes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00781Aspects relating to microreactors
    • B01J2219/0095Control aspects
    • B01J2219/00952Sensing operations
    • B01J2219/00954Measured properties
    • B01J2219/00961Temperature
    • 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
    • C07F9/06Phosphorus compounds without P—C bonds
    • C07F9/16Esters of thiophosphoric acids or thiophosphorous acids
    • C07F9/165Esters of thiophosphoric acids
    • C07F9/20Esters of thiophosphoric acids containing P-halide groups
    • C07F9/2003Esters of thiophosphoric acids containing P-halide groups containing the structure Hal-P-X-unsaturated acyclic group

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Luminescent Compositions (AREA)

Abstract

La presente divulgación se refiere a un proceso continuo para la producción de acefato, comprendiendo dicho proceso las etapas de: poner en contacto fosforoamidotioato de O,O-dimetilo con sulfato de dimetilo para obtener metamidofos; poner en contacto metamidofos con un agente acetilante para obtener acefato. Reivindicación 1: Un proceso para la producción de acefato que comprende a) hacer reaccionar fosforamidotioato de O,O-dimetilo y sulfato de dimetilo para obtener metamidofos y b) convertir metamidofos en acefato en el que dicho proceso es un proceso continuo y las etapas se realizan en un sistema de flujo continuo. Reivindicación 2: El proceso según la reivindicación 1, en el que dicho proceso se realiza a una temperatura que varía de 50ºC a 100ºC. Reivindicación 3: El proceso según la reivindicación 1, en el que el tiempo de residencia de los reactivos en el proceso es de aproximadamente 30 segundos a 1 hora. Reivindicación 4: El proceso según la reivindicación 1 que comprende además convertir metamidofos en acefato poniendo en contacto metamidofos con un agente acetilante en un reactor de flujo continuo para obtener acefato. Reivindicación 13: Un proceso para la producción de fosforoamidotioato de O,O-dimetilo que comprende poner en contacto fosforodicloridotioato de O-metilo con sosa cáustica continuamente en un reactor de flujo avanzado para formar fosforocloridotioato de O,O-dimetilo; y poner en contacto fosforocloridotioato de O,O-dimetilo con una solución de amoniaco continuamente en un reactor de flujo avanzado para formar fosforoamidotioato de O,O-dimetilo. Reivindicación 14: El proceso según la reivindicación 13, en el que la solución de amoniaco se pone en contacto con fosforocloridotioato de O,O-dimetilo a una temperatura que varía de 25ºC a 45ºC. Reivindicación 15: El proceso según la reivindicación 13, en el que la solución de amoniaco comprende NH₃ del 12 al 20%.
ARP220100402A 2021-02-25 2022-02-24 Un proceso para la producción de acefato AR124965A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IN202121008039 2021-02-25

Publications (1)

Publication Number Publication Date
AR124965A1 true AR124965A1 (es) 2023-05-24

Family

ID=82976083

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP220100402A AR124965A1 (es) 2021-02-25 2022-02-24 Un proceso para la producción de acefato

Country Status (4)

Country Link
CN (1) CN114957318A (es)
AR (1) AR124965A1 (es)
BR (1) BR112023017031A2 (es)
WO (1) WO2022180555A1 (es)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116396325B (zh) * 2023-02-01 2023-09-15 浙江泰达作物科技有限公司 一种连续流微反应器高效制备乙酰甲胺磷的方法

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3291987B2 (ja) * 1995-08-07 2002-06-17 住友化学工業株式会社 O,s−ジメチル−n−アセチルホスホルアミドチオエートの精製法
CN1215769C (zh) * 2002-01-28 2005-08-24 湘潭大学 乙酰甲胺磷可溶粉的制备方法
CN1169817C (zh) * 2002-01-28 2004-10-06 湘潭大学 高纯度乙酰甲胺磷原粉的制备方法(2)
CN1176929C (zh) * 2002-01-28 2004-11-24 湘潭大学 高纯度乙酰甲胺磷原粉的制备方法
CN101289462B (zh) * 2007-04-20 2010-12-01 济南大学 由乙烯酮制备乙酰甲胺磷的方法
CN100506832C (zh) * 2007-06-25 2009-07-01 山东汇海医药化工有限公司 一种制备乙酰甲胺磷的方法
IN2010CH00118A (es) * 2010-01-18 2012-05-25 Hamamapure B.B Dr.
US10669295B2 (en) * 2018-07-19 2020-06-02 Arysta Lifescience Inc. Process for preparation of O,O-dimethyl phosphoramidothioate and N-(methoxy-methylsulfanylphosphoryl) acetamide
WO2021152443A1 (en) * 2020-01-31 2021-08-05 Upl Limited A continuous flow process for preparation of acephate and its intermediates

Also Published As

Publication number Publication date
WO2022180555A1 (en) 2022-09-01
CN114957318A (zh) 2022-08-30
BR112023017031A2 (pt) 2023-09-26

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