ES2040608T3 - Procedimiento para la produccion de mezclas de acetales ciclicos de acroleina con glicerol. - Google Patents

Procedimiento para la produccion de mezclas de acetales ciclicos de acroleina con glicerol.

Info

Publication number
ES2040608T3
ES2040608T3 ES199191118213T ES91118213T ES2040608T3 ES 2040608 T3 ES2040608 T3 ES 2040608T3 ES 199191118213 T ES199191118213 T ES 199191118213T ES 91118213 T ES91118213 T ES 91118213T ES 2040608 T3 ES2040608 T3 ES 2040608T3
Authority
ES
Spain
Prior art keywords
acrolein
glycerol
acetals
reaction
blends
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.)
Expired - Lifetime
Application number
ES199191118213T
Other languages
English (en)
Inventor
Mathias Dr. Hopp
Dietrich Dr. Arntz
Stephan Dr. Bartsch
Adolf Dr. Schafer-Sindlinger
Wolfgang Dr. Bock
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
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 Degussa GmbH filed Critical Degussa GmbH
Application granted granted Critical
Publication of ES2040608T3 publication Critical patent/ES2040608T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D319/00Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D319/041,3-Dioxanes; Hydrogenated 1,3-dioxanes
    • C07D319/061,3-Dioxanes; Hydrogenated 1,3-dioxanes not condensed with other rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D317/00Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/10Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
    • C07D317/14Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D317/18Radicals substituted by singly bound oxygen or sulfur atoms
    • C07D317/20Free hydroxyl or mercaptan

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Saccharide Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

LAS MEZCLAS DE ACROLELINGLICENACETALE CICLICAS SE OBTIENEN MEDIANTE LA TRANSFORMACION DE ACROLEINA CON GLICERINA EN PRESENCIA DE UN CATALIZADOR ACIDO Y SOLIDO. PARA QUE LAS MEZCLAS OBTENIDAS SEAN DE UN ALTO PODER SELECTIVO SE DEBE DE EFECTUAR LA TRANSFORMACION EN PRESENCIA DE UNA MEZCLA DE REACCION A MODO DE DISOLVENTE QUE CONSTE DE AGUA, ACROLEINGLICERINACETALEN CICLICOS, GLICERINA Y DE ACROLEINA Y, CON LA NO PRESENCIA DE DISOLVENTES EXTRAÑOS, AÑADIENDO LA MEZCLA DE REACCION LIBERADA DEL CATALIZADOR ANTES DE LA PREPARACION DESTILADA CON UNA SUSTANCIA AUMENTADA AL VALOR PH, DE TAL FORMA QUE LA MEZCLA TENGA UN VALOR 10 VECES MAS DE UN VALOR PH DE LA DILUCION CON AGUA, DENTRO DEL MARGENDE 4, 5 A 7. PREFERIBLEMENTE LA TRANSFORMACION SE LLEVA A CABO A UNA TEMPERATURA DE 10 A 30 C, UTILIZANDO UN INTERCAMBIADOR DE IONES FUERTEMENTE ORGANICO O INORGANICO.
ES199191118213T 1990-12-17 1991-10-25 Procedimiento para la produccion de mezclas de acetales ciclicos de acroleina con glicerol. Expired - Lifetime ES2040608T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE4040362A DE4040362A1 (de) 1990-12-17 1990-12-17 Verfahren zur herstellung von gemischen cyclischer acroleinglycerinacetale

Publications (1)

Publication Number Publication Date
ES2040608T3 true ES2040608T3 (es) 1993-10-16

Family

ID=6420582

Family Applications (1)

Application Number Title Priority Date Filing Date
ES199191118213T Expired - Lifetime ES2040608T3 (es) 1990-12-17 1991-10-25 Procedimiento para la produccion de mezclas de acetales ciclicos de acroleina con glicerol.

Country Status (10)

Country Link
US (1) US5216179A (es)
EP (1) EP0491142B1 (es)
JP (1) JPH04266884A (es)
AT (1) ATE89824T1 (es)
AU (1) AU634919B2 (es)
CA (1) CA2057740A1 (es)
DE (2) DE4040362A1 (es)
DK (1) DK0491142T3 (es)
ES (1) ES2040608T3 (es)
IL (1) IL100381A0 (es)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX9602980A (es) * 1994-01-25 1997-03-29 Du Pont Proceso mejorado para la sintesis de compuestos de dioxovinilo.
DE4431994A1 (de) * 1994-09-08 1996-03-14 Degussa Verfahren zur Herstellung von 1,1,3-Trialkoxypropan
DE4435009A1 (de) * 1994-09-30 1996-04-04 Degussa Verfahren zur Herstellung von 2-Vinyl-1,3-dioxolan
EP1905767A1 (de) * 2006-09-28 2008-04-02 Cognis IP Management GmbH Verfahren zur Herstellung von Glycerinacetalen
FR2925490B1 (fr) * 2007-12-20 2009-12-25 Arkema France Procede de synthese d'acroleine a partir de glycerol

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3014924A (en) * 1958-04-15 1961-12-26 Du Pont Catalytic process for making unsaturated cyclic acetals
US3250788A (en) * 1962-08-01 1966-05-10 Union Carbide Corp Process for making 4-(4-hydroxybutyl)-2-vinyl-1, 3-dioxolane
US4003918A (en) * 1975-12-15 1977-01-18 Celanese Corporation Production of 2-vinyl-1,3-dioxane compounds

Also Published As

Publication number Publication date
DE4040362A1 (de) 1992-06-25
US5216179A (en) 1993-06-01
EP0491142B1 (de) 1993-05-26
DE59100132D1 (de) 1993-07-01
AU8973691A (en) 1992-06-18
DK0491142T3 (da) 1993-07-12
AU634919B2 (en) 1993-03-04
JPH04266884A (ja) 1992-09-22
IL100381A0 (en) 1992-09-06
EP0491142A1 (de) 1992-06-24
CA2057740A1 (en) 1992-06-18
ATE89824T1 (de) 1993-06-15

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