[go: up one dir, main page]

FR2217372A1 - Low mol wt polyglycidyl ethers prepn. - by catalytic etherification of polyvalent phenols with epihalohydrins - Google Patents

Low mol wt polyglycidyl ethers prepn. - by catalytic etherification of polyvalent phenols with epihalohydrins

Info

Publication number
FR2217372A1
FR2217372A1 FR7405063A FR7405063A FR2217372A1 FR 2217372 A1 FR2217372 A1 FR 2217372A1 FR 7405063 A FR7405063 A FR 7405063A FR 7405063 A FR7405063 A FR 7405063A FR 2217372 A1 FR2217372 A1 FR 2217372A1
Authority
FR
France
Prior art keywords
alkali
treated
epihalohydrin
residue
distilled
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.)
Granted
Application number
FR7405063A
Other languages
French (fr)
Other versions
FR2217372B1 (en
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.)
Inventa AG fuer Forschung und Patentverwertung
Original Assignee
Inventa AG fuer Forschung und Patentverwertung
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 Inventa AG fuer Forschung und Patentverwertung filed Critical Inventa AG fuer Forschung und Patentverwertung
Publication of FR2217372A1 publication Critical patent/FR2217372A1/en
Application granted granted Critical
Publication of FR2217372B1 publication Critical patent/FR2217372B1/fr
Granted legal-status Critical Current

Links

Classifications

    • 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
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/02Polycondensates containing more than one epoxy group per molecule
    • C08G59/04Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof
    • C08G59/06Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols
    • C08G59/063Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols with epihalohydrins
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D303/00Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
    • C07D303/02Compounds containing oxirane rings
    • C07D303/12Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
    • C07D303/18Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified hydroxyl radicals
    • C07D303/20Ethers with hydroxy compounds containing no oxirane rings
    • C07D303/24Ethers with hydroxy compounds containing no oxirane rings with polyhydroxy compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Epoxy Compounds (AREA)
  • Epoxy Resins (AREA)
  • Polyethers (AREA)

Abstract

The polyvalent phenol is >=60% catalytically etherified (calc. on the no. of phenolic OH gps.) with 3-8 equiv. epihalohydrin per phenolic OH gp, and the mixture obtained is treated with org. alkali contg. 0.5-0.98 equiv. alkali cpd. per phenolic OH gp and of concn. which is not > than the saturation concn. of the salt produced by this alkali treatment at the temp. of the reaction mixture. In this process (a) the alkali treatment is effected at >=50 degrees C, the aqs. phase being separated, the epihalohydrin being distilled from the organic phase and the residue being post. treated with the aq. alkali, or (b) all or some of the epihalohydrin is distilled from the etherification mixture and the residue is treated with the aq alkali at >=50 degrees C, the aq. phase being separated and residual epihalohydrin from both the organic phase and from the prior alkali treatment distilled, and the residue being treated as in (a). Loss of epihalodrin is minimal, quality of opoxy resin produced from the polyglycidyl ethers is not reduced and no blockage of the tubes and pipes in the plant by pptd. salt, nor overheating occurs.
FR7405063A 1973-02-15 1974-02-14 Low mol wt polyglycidyl ethers prepn. - by catalytic etherification of polyvalent phenols with epihalohydrins Granted FR2217372A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH231973A CH575405A5 (en) 1973-02-15 1973-02-15

Publications (2)

Publication Number Publication Date
FR2217372A1 true FR2217372A1 (en) 1974-09-06
FR2217372B1 FR2217372B1 (en) 1976-11-26

Family

ID=4231025

Family Applications (1)

Application Number Title Priority Date Filing Date
FR7405063A Granted FR2217372A1 (en) 1973-02-15 1974-02-14 Low mol wt polyglycidyl ethers prepn. - by catalytic etherification of polyvalent phenols with epihalohydrins

Country Status (6)

Country Link
JP (1) JPS5213840B2 (en)
BR (1) BR7401083D0 (en)
CH (1) CH575405A5 (en)
DE (1) DE2407092B2 (en)
ES (1) ES423191A1 (en)
FR (1) FR2217372A1 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009120685A3 (en) * 2008-03-25 2009-11-19 Dow Global Technologies Inc. Process for manufacturing liquid epoxy resins
FR2954772A1 (en) * 2009-12-24 2011-07-01 Solvay Manufacturing epoxy resin involves reacting epichlorohydrin with aromatic polyol to form the epoxy resin and salt, and in which use is made of non-halogenated, non-aromatic alcohol, as additive, added to/formed in step of the process
US9663427B2 (en) 2003-11-20 2017-05-30 Solvay (Société Anonyme) Process for producing epichlorohydrin

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE872673A (en) * 1977-12-20 1979-06-12 Shell Int Research PROCESS FOR PREPARING POLYGLYCIDYL ETHERS
DE2947469A1 (en) * 1979-11-24 1981-06-04 Hoechst Ag, 6000 Frankfurt METHOD FOR THE PRODUCTION OF GLYCIDYL ETHERS OF UNIFORM OR MULTIPLE VALUES
SE457726B (en) * 1980-12-18 1989-01-23 Sumitomo Chemical Co ZINC POWDER COATING COATING AND POLYHYDROXYETER
JPS58198476A (en) * 1982-05-14 1983-11-18 Kanegafuchi Chem Ind Co Ltd Preparation of polyglycidyl derivative
JPS60210622A (en) * 1984-04-05 1985-10-23 Sanyo Kokusaku Pulp Co Ltd Manufacturing method of high purity flame retardant epoxy resin
KR20080037615A (en) 2005-05-20 2008-04-30 솔베이(소시에떼아노님) Method for producing chlorohydrin
WO2006106154A1 (en) 2005-05-20 2006-10-12 Solvay (Société Anonyme) Continuous method for making chlorhydrines
KR100979372B1 (en) 2006-06-14 2010-08-31 솔베이(소시에떼아노님) Crude glycerol-based product, its purification method and its use for preparing dichloropropanol
FR2913421B1 (en) 2007-03-07 2009-05-15 Solvay PROCESS FOR PRODUCING DICHLOROPROPANOL
FR2913684B1 (en) 2007-03-14 2012-09-14 Solvay PROCESS FOR PRODUCING DICHLOROPROPANOL
TW200911740A (en) 2007-06-01 2009-03-16 Solvay Process for manufacturing a chlorohydrin
TW200911693A (en) 2007-06-12 2009-03-16 Solvay Aqueous composition containing a salt, manufacturing process and use
TW200911773A (en) 2007-06-12 2009-03-16 Solvay Epichlorohydrin, manufacturing process and use
EP2207617A1 (en) 2007-10-02 2010-07-21 SOLVAY (Société Anonyme) Use of compositions containing silicon for improving the corrosion resistance of vessels
FR2925045B1 (en) 2007-12-17 2012-02-24 Solvay GLYCEROL-BASED PRODUCT, PROCESS FOR OBTAINING THE SAME AND USE THEREOF IN THE MANUFACTURE OF DICHLOROPROPANOL
TWI478875B (en) 2008-01-31 2015-04-01 Solvay Process for degrading organic substances in an aqueous composition
EA201071157A1 (en) 2008-04-03 2011-04-29 Солвей (Сосьете Аноним) COMPOSITION CONTAINING GLYCERIN, METHOD OF ITS RECEPTION AND APPLICATION IN PRODUCTION OF DICHLORPROPANOL
FR2935968B1 (en) 2008-09-12 2010-09-10 Solvay PROCESS FOR THE PURIFICATION OF HYDROGEN CHLORIDE
WO2011054770A1 (en) * 2009-11-04 2011-05-12 Solvay Sa Process for manufacturing an epoxy resin
EP2621911A1 (en) 2010-09-30 2013-08-07 Solvay Sa Derivative of epichlorohydrin of natural origin

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
NEANT *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9663427B2 (en) 2003-11-20 2017-05-30 Solvay (Société Anonyme) Process for producing epichlorohydrin
WO2009120685A3 (en) * 2008-03-25 2009-11-19 Dow Global Technologies Inc. Process for manufacturing liquid epoxy resins
US8461286B2 (en) 2008-03-25 2013-06-11 Dow Global Technologies Llc Process for manufacturing liquid epoxy resins
FR2954772A1 (en) * 2009-12-24 2011-07-01 Solvay Manufacturing epoxy resin involves reacting epichlorohydrin with aromatic polyol to form the epoxy resin and salt, and in which use is made of non-halogenated, non-aromatic alcohol, as additive, added to/formed in step of the process

Also Published As

Publication number Publication date
DE2407092C3 (en) 1979-03-29
DE2407092B2 (en) 1978-07-27
CH575405A5 (en) 1976-05-14
FR2217372B1 (en) 1976-11-26
BR7401083D0 (en) 1974-11-05
JPS5213840B2 (en) 1977-04-16
JPS49114697A (en) 1974-11-01
ES423191A1 (en) 1976-09-16
DE2407092A1 (en) 1974-09-05

Similar Documents

Publication Publication Date Title
FR2217372A1 (en) Low mol wt polyglycidyl ethers prepn. - by catalytic etherification of polyvalent phenols with epihalohydrins
KR0175324B1 (en) Process to reduce propenyl polyethers in hydroxy-functional polyethers
KR910007854A (en) Method of producing monoepoxide
KR0170383B1 (en) Process for producing propenyl ether concentration in hydroxy-functional polyether compounds
GB1493538A (en) Preparation of glycide ethers
US5245048A (en) Production of glycidyl compounds
KR930004793B1 (en) Process for reducing the content of hydrolyzable chlorine in glycidyl compound
ES8400469A1 (en) Solid epoxide resin.
GB986250A (en) Process for the preparation of polygylcidyl ethers of polyhydric phenols
KR950704391A (en) Process for producing a high molecular weight epoxy resin
GB590883A (en) Improvements in and relating to cation-exchange resins for removing cations from liquid media
US2892849A (en) Process for preparing epoxyalkyl aryl ethers
FR2281951A1 (en) Hardening internal polyepoxides using trivalent chromium catalyst - with polycarboxylic acid hardener, active at low temp.
GB1277668A (en) Improved method of making glycidyl ethers
JPS56116717A (en) Preparation of novolak-type epoxy resin
ES454385A1 (en) Preparation of novolak epoxy resins
US3023225A (en) Xchxch
BE810180A (en) Glycidyl ethers of mono/polyvalent phenols - by reacting phenol with epichlorohydrin, and treating prod with alkali metal hydroxide in two stages
FR2490654B1 (en)
JPS57170922A (en) Preparation of solid epoxy resin
GB1159530A (en) Process for the Manufacture of Glycidyl Ethers of Polyhydricphenols with a High Content of Epoxide Oxygen
GB1124320A (en) Production of glycidol and glycerine
GB1065546A (en) Improvements in and relating to epoxy resins
GB1115186A (en) Epoxidation process
US3642911A (en) Process for preparing aryloxyalkanols

Legal Events

Date Code Title Description
ST Notification of lapse