BR112018009801A8 - métodos para preparar um éster de ácido 3-hidroxipropiônico e um éster de ácido acrílico. - Google Patents

métodos para preparar um éster de ácido 3-hidroxipropiônico e um éster de ácido acrílico.

Info

Publication number
BR112018009801A8
BR112018009801A8 BR112018009801A BR112018009801A BR112018009801A8 BR 112018009801 A8 BR112018009801 A8 BR 112018009801A8 BR 112018009801 A BR112018009801 A BR 112018009801A BR 112018009801 A BR112018009801 A BR 112018009801A BR 112018009801 A8 BR112018009801 A8 BR 112018009801A8
Authority
BR
Brazil
Prior art keywords
acid ester
preparing
methods
hydroxypropionic acid
acrylic acid
Prior art date
Application number
BR112018009801A
Other languages
English (en)
Other versions
BR112018009801A2 (pt
Inventor
Linder David
Pazicky Marek
Blanchot Mathieu
Paciello Rocco
Fischer Wolfgang
Original Assignee
Basf Se
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 Basf Se filed Critical Basf Se
Publication of BR112018009801A2 publication Critical patent/BR112018009801A2/pt
Publication of BR112018009801A8 publication Critical patent/BR112018009801A8/pt

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/03Preparation of carboxylic acid esters by reacting an ester group with a hydroxy group
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/30Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/317Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups
    • C07C67/327Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups by elimination of functional groups containing oxygen only in singly bound form
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0215Sulfur-containing compounds
    • B01J31/0225Sulfur-containing compounds comprising sulfonic acid groups or the corresponding salts
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/52Esters of acyclic unsaturated carboxylic acids having the esterified carboxyl group bound to an acyclic carbon atom
    • C07C69/533Monocarboxylic acid esters having only one carbon-to-carbon double bond
    • C07C69/54Acrylic acid esters; Methacrylic acid esters
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/66Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
    • C07C69/67Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids
    • C07C69/675Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids of saturated hydroxy-carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/06Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from hydroxycarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/78Preparation processes
    • C08G63/82Preparation processes characterised by the catalyst used
    • C08G63/823Preparation processes characterised by the catalyst used for the preparation of polylactones or polylactides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/40Substitution reactions at carbon centres, e.g. C-C or C-X, i.e. carbon-hetero atom, cross-coupling, C-H activation or ring-opening reactions
    • B01J2231/49Esterification or transesterification
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/40Complexes comprising metals of Group IV (IVA or IVB) as the central metal
    • B01J2531/46Titanium
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/347Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
    • C07C51/377Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Catalysts (AREA)

Abstract

a invenção refere-se a ésteres de ácido 3-hidroxipropiônico, obtidos por conversão de óxido de etileno com monóxido de carbono na presença de um catalisador de cobalto, em que poli-3-hidroxipropionato é obtido; e transesterificação do poli-3-hidroxipropionato com um álcool na presença de um catalisador de transesterificação, em que os ésteres de ácido 3-hidroxipropiônico são obtidos. o catalisador de transesterificação é um composto da fórmula mlx, em que m representa um metal do 2º, 3º, ou 4º grupo principal ou do grupo secundário 3º a 8º da tabela periódica dos elementos, l representa um ligante, o qual se liga diretamente a um m por meio de um átomo c, um o, um p, um s e/ou um n, e x é um número inteiro de 2 a 6.
BR112018009801A 2015-11-17 2016-11-16 métodos para preparar um éster de ácido 3-hidroxipropiônico e um éster de ácido acrílico. BR112018009801A8 (pt)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201562256161P 2015-11-17 2015-11-17
DE102015222675 2015-11-17
PCT/EP2016/077851 WO2017085120A1 (de) 2015-11-17 2016-11-16 Herstellung von estern der 3-hydroxypropionsäure und acrylsäure

Publications (2)

Publication Number Publication Date
BR112018009801A2 BR112018009801A2 (pt) 2018-11-06
BR112018009801A8 true BR112018009801A8 (pt) 2019-02-26

Family

ID=58717405

Family Applications (1)

Application Number Title Priority Date Filing Date
BR112018009801A BR112018009801A8 (pt) 2015-11-17 2016-11-16 métodos para preparar um éster de ácido 3-hidroxipropiônico e um éster de ácido acrílico.

Country Status (7)

Country Link
US (1) US20180327345A1 (pt)
EP (1) EP3377554A1 (pt)
JP (1) JP2018536712A (pt)
KR (1) KR20180085746A (pt)
CN (1) CN108350158A (pt)
BR (1) BR112018009801A8 (pt)
WO (1) WO2017085120A1 (pt)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111100000B (zh) * 2018-10-25 2022-07-12 中国石油化工股份有限公司 钴催化合成3-羟基丙酸甲酯的方法
CN114425451B (zh) * 2020-10-14 2024-01-30 中国石油化工股份有限公司 一种合成3-羟基丙酸酯的催化剂及其制备和使用方法
CN114289067B (zh) * 2021-12-30 2023-04-04 厦门大学 二元金属催化剂、制备方法及其应用

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10137046A1 (de) 2001-07-31 2003-02-20 Basf Ag Verfahren zur Herstellung von thermoplastischen Poly(3-hydroxyalkanoaten)
DE10149269A1 (de) 2001-10-05 2003-07-31 Basf Ag Verfahren zur Herstellung von Poly(3-hydroxyalkanoaten)
US6844447B2 (en) 2001-12-18 2005-01-18 Metabolix Inc. Methods of making intermediates from polyhydroxyalkanoates
CN100577628C (zh) * 2002-03-25 2010-01-06 嘉吉有限公司 制造β-羟基羧酸衍生物的方法
WO2005095320A1 (en) 2004-04-02 2005-10-13 Ciba Specialty Chemicals Water Treatments Limited Preparation of acrylic acid derivatives from alpha or beta-hydroxy carboxylic acids
DE102006039203B4 (de) 2006-08-22 2014-06-18 Evonik Degussa Gmbh Verfahren zur Herstellung von durch Kristallisation gereinigter Acrylsäure aus Hydroxypropionsäure sowie Vorrichtung dazu
CN104350034B (zh) 2012-06-08 2018-07-31 Cj 第一制糖株式会社 可再生丙烯酸生产和自其制备的产物
DE102012212437A1 (de) 2012-07-16 2014-01-16 Basf Se Verfahren zur Herstellung von Acrylsäure aus Ethylenoxid und Kohlenmonoxid
WO2015036218A1 (de) 2013-09-12 2015-03-19 Basf Se Verfahren zur dehydratisierung von 3-hydroxypropionsäure zu acrylsäure
US9630900B2 (en) 2013-09-12 2017-04-25 Basf Se Method for the dehydration of 3-hydroxypropanoic acid to form acrylic acid

Also Published As

Publication number Publication date
JP2018536712A (ja) 2018-12-13
EP3377554A1 (de) 2018-09-26
BR112018009801A2 (pt) 2018-11-06
WO2017085120A1 (de) 2017-05-26
US20180327345A1 (en) 2018-11-15
CN108350158A (zh) 2018-07-31
KR20180085746A (ko) 2018-07-27

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B11Y Definitive dismissal - extension of time limit for request of examination expired [chapter 11.1.1 patent gazette]