GB854952A - Polyglycol ethers - Google Patents

Polyglycol ethers

Info

Publication number
GB854952A
GB854952A GB33611/57A GB3361157A GB854952A GB 854952 A GB854952 A GB 854952A GB 33611/57 A GB33611/57 A GB 33611/57A GB 3361157 A GB3361157 A GB 3361157A GB 854952 A GB854952 A GB 854952A
Authority
GB
United Kingdom
Prior art keywords
reaction
ethylene oxide
naphthol
phenylethyl
phenol
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
Application number
GB33611/57A
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.)
Bayer AG
Original Assignee
Bayer AG
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 Bayer AG filed Critical Bayer AG
Publication of GB854952A publication Critical patent/GB854952A/en
Expired 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
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/26Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
    • C08G65/2603Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen
    • C08G65/2606Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups
    • C08G65/2612Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups containing aromatic or arylaliphatic hydroxyl groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Polyglycol ethers, are produced by reacting 10 to 20 mols of an oxyalkylating agent, such as ethylene oxide, with 1 mol of a product obtained by the addition-reaction between styrene, vinyltoluene, a -methylstyrene or divinylbenzene, and the aromatic nucleus of a phenol or a naphthol. In Example 3, a mixture of mono-, di-, and tri-a -phenylethylphenol, obtained by reacting 2 mols of styrene with 1 mol of phenol in the presence of sulphuric acid, is reacted at 120 DEG -130 DEG C. with ethylene oxide in the presence of caustic potash, the liquid ethylene oxide (540 parts) being run into the mixture of a -phenylethylphenols while maintaining in the reaction-vessel a gauge-pressure of about 2 atm. The reaction-product is a water-soluble oil, which may be used to convert water-insoluble pesticides into clear aqueous emulsions (see Group VI). Other examples relate to the reaction of the ethylene oxide with a -phenylethyl-p-hydroxydiphenyl, di-a -phenylethyl-cresol, mono-a -phenylethyl-naphthol, and di-phenylisopropylphenol.ALSO:Water-insoluble pesticides of the thionophosphoric-O,O-dialkyl-O-p-nitrophenyl ester type are converted into clear aqueous emulsions by means of polyglycol ethers produced by reacting an oxyalkylating agent, such as ethylene oxide, with a product obtained by the addition-reaction between styrene (or a derivative thereof) and the aromatic nucleus of a phenol or a naphthol (see Group IV(b)).
GB33611/57A 1956-11-03 1957-10-28 Polyglycol ethers Expired GB854952A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE854952X 1956-11-03

Publications (1)

Publication Number Publication Date
GB854952A true GB854952A (en) 1960-11-23

Family

ID=6788979

Family Applications (1)

Application Number Title Priority Date Filing Date
GB33611/57A Expired GB854952A (en) 1956-11-03 1957-10-28 Polyglycol ethers

Country Status (1)

Country Link
GB (1) GB854952A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4127550A (en) * 1976-11-03 1978-11-28 Milliken Research Corporation Method for improving the scrub-resistant properties of water-based latex paint compositions
US4322312A (en) * 1978-12-16 1982-03-30 Bayer Aktiengesellschaft Process for purification of non-ionic emulsifiers
US5154754A (en) * 1987-03-11 1992-10-13 Hoechst Aktiengesellschaft Oil-in-water emulsions and a process for their preparation and their use
US5855662A (en) * 1995-03-30 1999-01-05 Bayer Aktiengesellschaft Aqueous pigment preparations
EP3208293A1 (en) * 2016-02-17 2017-08-23 Clariant International Ltd Alkoxylated phenol derivatives

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4127550A (en) * 1976-11-03 1978-11-28 Milliken Research Corporation Method for improving the scrub-resistant properties of water-based latex paint compositions
US4322312A (en) * 1978-12-16 1982-03-30 Bayer Aktiengesellschaft Process for purification of non-ionic emulsifiers
US5154754A (en) * 1987-03-11 1992-10-13 Hoechst Aktiengesellschaft Oil-in-water emulsions and a process for their preparation and their use
US5855662A (en) * 1995-03-30 1999-01-05 Bayer Aktiengesellschaft Aqueous pigment preparations
EP3208293A1 (en) * 2016-02-17 2017-08-23 Clariant International Ltd Alkoxylated phenol derivatives
WO2017140508A1 (en) * 2016-02-17 2017-08-24 Clariant International Ltd Alkoxylated phenol derivatives
CN108699234A (en) * 2016-02-17 2018-10-23 科莱恩国际有限公司 Alkoxylated amphyl

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