EP1984319A1 - Procede de fabrication d'amines par conditionnement d'un catalyseur avec de l'ammoniac - Google Patents

Procede de fabrication d'amines par conditionnement d'un catalyseur avec de l'ammoniac

Info

Publication number
EP1984319A1
EP1984319A1 EP06819836A EP06819836A EP1984319A1 EP 1984319 A1 EP1984319 A1 EP 1984319A1 EP 06819836 A EP06819836 A EP 06819836A EP 06819836 A EP06819836 A EP 06819836A EP 1984319 A1 EP1984319 A1 EP 1984319A1
Authority
EP
European Patent Office
Prior art keywords
catalyst
ammonia
conditioning
catalysts
starting compounds
Prior art date
Legal status (The legal status 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 status listed.)
Withdrawn
Application number
EP06819836A
Other languages
German (de)
English (en)
Inventor
Christian Lettmann
Juergen Lippe
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Evonik Operations GmbH
Original Assignee
Evonik Degussa GmbH
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 Evonik Degussa GmbH filed Critical Evonik Degussa GmbH
Publication of EP1984319A1 publication Critical patent/EP1984319A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C209/00Preparation of compounds containing amino groups bound to a carbon skeleton
    • C07C209/24Preparation of compounds containing amino groups bound to a carbon skeleton by reductive alkylation of ammonia, amines or compounds having groups reducible to amino groups, with carbonyl compounds
    • C07C209/26Preparation of compounds containing amino groups bound to a carbon skeleton by reductive alkylation of ammonia, amines or compounds having groups reducible to amino groups, with carbonyl compounds by reduction with hydrogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C209/00Preparation of compounds containing amino groups bound to a carbon skeleton
    • C07C209/44Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of carboxylic acids or esters thereof in presence of ammonia or amines, or by reduction of nitriles, carboxylic acid amides, imines or imino-ethers
    • C07C209/48Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of carboxylic acids or esters thereof in presence of ammonia or amines, or by reduction of nitriles, carboxylic acid amides, imines or imino-ethers by reduction of nitriles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/12Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14The ring being saturated

Definitions

  • the conditioning can be carried out in a wide temperature range. Usually, at temperatures between 20 and 180 0 C, preferably 50 to 130 0 C, worked. Particularly preferably, a temperature ramp is passed through, in which the catalyst, starting at a moderately elevated temperature, preferably between 20 and 50 0 C, slowly up to the desired later for the hydrogenation reaction temperature, preferably 50 to 130 0 C, heated.
  • the diamine yield is 3% higher than without conditioning. This is due, on the one hand, to the higher conversion (less intermediate isophorone aminonitrile in the product) and, on the other hand, to the higher selectivity (lower proportion of the cyclic by-products amidine and imine).
  • the experiments were carried out in a 1 L hydrogenation autoclave equipped with a catalyst basket (static basket with stirrer, "Mahoney type").
  • the catalyst basket was filled in each case freshly with 80 mL of a spherical cobalt Raneytyp fixed-bed catalyst.
  • the reactor was first filled with about 500 ml of ammonia and kept under stirring for about 2 h at 50 0 C and 250 bar. Thereafter, the ammonia was vented by venting the reactor.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

L'invention concerne un procédé de fabrication d'amines par conditionnement d'un catalyseur avec de l'ammoniac.
EP06819836A 2006-02-14 2006-11-29 Procede de fabrication d'amines par conditionnement d'un catalyseur avec de l'ammoniac Withdrawn EP1984319A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102006006625A DE102006006625A1 (de) 2006-02-14 2006-02-14 Verfahren zur Herstellung von Aminen durch Konditionierung des Katalysators mit Ammoniak
PCT/EP2006/069056 WO2007093240A1 (fr) 2006-02-14 2006-11-29 Procede de fabrication d'amines par conditionnement d'un catalyseur avec de l'ammoniac

Publications (1)

Publication Number Publication Date
EP1984319A1 true EP1984319A1 (fr) 2008-10-29

Family

ID=37719254

Family Applications (1)

Application Number Title Priority Date Filing Date
EP06819836A Withdrawn EP1984319A1 (fr) 2006-02-14 2006-11-29 Procede de fabrication d'amines par conditionnement d'un catalyseur avec de l'ammoniac

Country Status (5)

Country Link
US (1) US20090048466A1 (fr)
EP (1) EP1984319A1 (fr)
CN (1) CN101020641A (fr)
DE (1) DE102006006625A1 (fr)
WO (1) WO2007093240A1 (fr)

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FR2850966B1 (fr) 2003-02-10 2005-03-18 Rhodia Polyamide Intermediates Procede de fabrication de composes dinitriles
FR2854891B1 (fr) 2003-05-12 2006-07-07 Rhodia Polyamide Intermediates Procede de preparation de dinitriles
EP1948591A1 (fr) 2005-10-18 2008-07-30 INVISTA Technologies S.à.r.l. Procede de preparation de 3-aminopentanenitrile
BRPI0709313A2 (pt) 2006-03-17 2011-07-05 Invista Tech Sarl método de separação e método para a preparação de triorganofosfitos
US7919646B2 (en) 2006-07-14 2011-04-05 Invista North America S.A R.L. Hydrocyanation of 2-pentenenitrile
DE102007011484A1 (de) 2007-03-07 2008-09-11 Evonik Degussa Gmbh Verfahren zur Herstellung von Trimethylhexamethylendiamin
DE102007011483A1 (de) * 2007-03-07 2008-09-18 Evonik Degussa Gmbh Verfahren zur Herstellung von 3-Aminomethyl-3,5,5-trimethylcyclohexylamin
CN101687658B (zh) 2007-05-14 2013-07-24 因温斯特技术公司 高效反应器和方法
WO2008157218A1 (fr) 2007-06-13 2008-12-24 Invista Technologies S.A.R.L. Procédé pour améliorer la qualité de l'adiponitrile
EP2229353B1 (fr) 2008-01-15 2018-01-03 INVISTA Textiles (U.K.) Limited Hydrocyanation de pentènenitriles
CN101910119B (zh) 2008-01-15 2013-05-29 因温斯特技术公司 用于制备和精制3-戊烯腈,和用于精制2-甲基-3-丁烯腈的方法
WO2010026920A1 (fr) * 2008-09-08 2010-03-11 三菱瓦斯化学株式会社 Procédé de production de xylylènediamine
JP5619753B2 (ja) 2008-10-14 2014-11-05 インヴィスタテクノロジーズ エスアエルエル 2−第二級−アルキル−4,5−ジ−(直鎖−アルキル)フェノール類を製造する方法
EP2488482B1 (fr) * 2009-07-31 2015-08-19 Dow Global Technologies LLC Procédé destiné à améliorer l'activité catalytique de systèmes catalyseurs pour l'amination réductrice de cyano-aldéhydes aliphatiques en diamines aliphatiques
CN102471231B (zh) * 2009-07-31 2015-01-07 陶氏环球技术有限责任公司 脂环族二胺及其制备方法
CN102482198B (zh) * 2009-07-31 2016-06-15 陶氏环球技术有限责任公司 将还原性氨化反应溶剂和杂质与一种或多种脂肪族二胺分离的方法
CN102471218B (zh) 2009-08-07 2014-11-05 因温斯特技术公司 用于形成二酯的氢化并酯化
CN102753604B (zh) * 2010-01-04 2015-01-21 罗地亚经营管理公司 多胺及其制造方法
DE102010038310A1 (de) 2010-07-23 2012-01-26 Evonik Degussa Gmbh Verfahren zur Herstellung von Diamino-dianhydro-dideoxy-hexitolen, besonders bevorzugt 2,5-Diamino-1,4:3,6-Dianhydro-2,5-Dideoxy-D-Hexitol
DE102010062587A1 (de) 2010-12-08 2012-06-14 Evonik Degussa Gmbh Verfahren zur Herstellung von Isophoron
DE102010062594B4 (de) 2010-12-08 2022-02-17 Evonik Operations Gmbh Verfahren zur Herstellung von 3-Aminomethyl-3,5,5-trimethylcyclohexylamin
DE102010062603A1 (de) 2010-12-08 2012-06-14 Evonik Degussa Gmbh Verfahren zur Herstellung von 3-Aminomethyl-3,5,5-trimethylcyclohexylamin
DE102011077681A1 (de) 2011-06-17 2012-12-20 Evonik Degussa Gmbh Verfahren zur Herstellung von 3-Cyano-3,5,5-trimethylcyclohexanon
CN102909035B (zh) * 2011-08-04 2014-07-02 上海泰禾化工有限公司 一种合成1,3-环己基二甲胺用催化剂及其制备方法
DE102012016433A1 (de) * 2012-08-17 2014-05-15 Oxea Gmbh Kontinuierliches Verfahren zur Herstellung primärer aliphatischer Amine aus Aldehyden
CN102924286B (zh) * 2012-10-31 2014-06-11 万华化学集团股份有限公司 一种n1-(2-氨乙基)-1,2-乙二胺的制备方法
CN105531254A (zh) 2013-09-13 2016-04-27 因温斯特技术公司 从二腈制造二胺的氢化方法
CN105555752A (zh) 2013-09-13 2016-05-04 因温斯特技术公司 使二腈氢化以便制备二胺
WO2015038679A1 (fr) 2013-09-13 2015-03-19 Invista Technologies S.A R.L. Préparation de catalyseur et procédé d'hydrogénation
WO2015038678A1 (fr) 2013-09-13 2015-03-19 Invista Technologies S.À R.L. Hydrogénation de dinitriles pour la préparation de diamines
WO2015038676A1 (fr) 2013-09-13 2015-03-19 Invista Technologies S.À R.L. Procédé d'hydrogénation pour la préparation de diamine à partir de dinitriles
WO2015164699A1 (fr) 2014-04-25 2015-10-29 Invista Technologies S.A R.L. Préparation de diamines par hydrogénation de dinitriles
CN106699611B (zh) * 2016-12-30 2018-11-13 沈阳化工研究院有限公司 一种连续加氢还原制备间氨基苯磺酸钠的生产方法
CN114433086B (zh) * 2020-10-30 2024-03-29 中国石油化工股份有限公司 具有催化醇临氢氨化合成有机胺功能的催化剂和载体及其制备方法和应用

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NL7408053A (nl) * 1973-09-12 1975-03-14 Ici Ltd Hydrogeneringskatalysator en werkwijze voor de bereiding daarvan.
AU513177B2 (en) * 1976-11-04 1980-11-20 Shell Internationale Research Maatschappij B.V. Preparing amines
CA1091700A (fr) * 1976-12-28 1980-12-16 John F. Van De Castle No translation available
DE19614154C1 (de) * 1996-04-10 1997-09-25 Basf Ag Verfahren zur gleichzeitigen Herstellung von 6-Aminocapronitril und Hexamethylendiamin
JP2001181384A (ja) * 1999-12-27 2001-07-03 Tosoh Corp ポリオキシアルキレンアミン製造触媒の再賦活化方法
DE10065030A1 (de) * 2000-12-23 2002-07-04 Degussa Verfahren zur Herstellung von 3-Aminomethyl-3,5,5-trimethylcyclohexylamin
DE10152135A1 (de) * 2001-10-23 2003-04-30 Basf Ag Cobalt-Trägerkatalysatoren für Nitrilhydrierungen
DE10231119A1 (de) * 2002-07-10 2004-02-05 Degussa Ag Verfahren zur Selektivitätserhöhung der Hydrierung von 4,4'-Diaminodiphenylmethan zu 4,4'-Diaminodicyclohexylmethan in Gegenwart eines N-Alkyl-4,4'-Diaminodiphenylmethans
DE102004023529A1 (de) * 2004-05-13 2005-12-08 Basf Ag Verfahren zur kontinuierlichen Herstellung eines Amins
DE102007011483A1 (de) * 2007-03-07 2008-09-18 Evonik Degussa Gmbh Verfahren zur Herstellung von 3-Aminomethyl-3,5,5-trimethylcyclohexylamin
DE102007011484A1 (de) * 2007-03-07 2008-09-11 Evonik Degussa Gmbh Verfahren zur Herstellung von Trimethylhexamethylendiamin

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Also Published As

Publication number Publication date
CN101020641A (zh) 2007-08-22
WO2007093240A1 (fr) 2007-08-23
US20090048466A1 (en) 2009-02-19
DE102006006625A1 (de) 2007-08-16

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