GB983814A - A method for preparing alkylene oxide polymers - Google Patents

A method for preparing alkylene oxide polymers

Info

Publication number
GB983814A
GB983814A GB21047/62A GB2104762A GB983814A GB 983814 A GB983814 A GB 983814A GB 21047/62 A GB21047/62 A GB 21047/62A GB 2104762 A GB2104762 A GB 2104762A GB 983814 A GB983814 A GB 983814A
Authority
GB
United Kingdom
Prior art keywords
sucrose
compounds
glycol
catalyst
exemplified
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
GB21047/62A
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.)
Takeda Pharmaceutical Co Ltd
Original Assignee
Takeda Chemical Industries Ltd
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 Takeda Chemical Industries Ltd filed Critical Takeda Chemical Industries Ltd
Publication of GB983814A publication Critical patent/GB983814A/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
    • C08G65/04Macromolecular 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 only
    • C08G65/06Cyclic ethers having no atoms other than carbon and hydrogen outside the ring
    • C08G65/08Saturated oxiranes
    • C08G65/10Saturated oxiranes characterised by the catalysts used
    • C08G65/12Saturated oxiranes characterised by the catalysts used containing organo-metallic compounds or metal hydrides

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

Alkylene oxide homopolymer and copolymers are made by polymerizing one or more alkylene oxides in the presence of a catalyst comprising the reaction product of an organometallic compound of the general formula M(R)n, where M is zinc or tin, n is an integer corresponding to the valency of M, and R is a C1 to C5 alkyl group, and an organic compound containing at least two hydroxyl groups and/or mercapto groups, or a hydroxyl group and a mercapto group. The polymerization may be effected in bulk or in a hydrocarbon or ether solvent. Specified alkylene oxides are ethylene, propylene, butylene, and styrene oxides, and butadiene monoxide. Exemplified organometallics are diethyl and diisobutyl zinc, and tetraethyl tin. The Specification contains an extensive list of suitable organic compounds. Exemplified compounds are sucrose, mono- and di-palmitate, ethylene glycol, butandiol, the monopotassium alcoholate of sucrose mono-palmitate, sucrose, glucose, sorbitol, sorbose, diacetone sorbose, pentaerythritol, glycol, polyethylene glycol, polypropylene glycol, polyvinyl alcohol, 2,6-di-(hydroxyethyl) pyridine, tri-(hydroxymethyl)-aminomethane, dimethylsilane diol, methylsilane triol, catechol, resorcinol, hydroquinone, pyrogallol, inositol, dihydroxynaphthol, thioglycol, and alizarine. After polymerization, the catalyst may be decomposed by aqueous methanol. The polymers have intrinsic viscosities of up to 20.ALSO:A polymerization catalyst for alkylene oxides comprises the reaction product of an organometallic compound of the general formula M(R)n wherein M is zinc or tin, n is an integer corresponding to the valency of M, and R is a C1-C5 alkyl group, and an organic compound containing at least two hydroxyl groups and/or mercapto groups or a hydroxyl group and a mercapto group. The organic compounds may be selected from polyhydric alcohols, phenols, thioalcohols and thiophenols, hydroxyalkyl mercaptides, polyalkylene glycols, polyvinyl alcohol, partially hydrolysed polyvinyl acetate, carbohydrates and derivatives thereof, hydroxy nitrogen-containing compounds, primary condensates of phenol and formaldehyde, and hydroxy silicon-containing compounds. The Specification contains an extensive list of these compounds. Exemplified compounds are sucrose mono- and dipalmitate, ethylene glycol, butandiol, the monopotassium alcoholate of sucrose monopalmitate, sucrose, glucose, sorbitol, sorbose, diacetone sorbose, pentaerythritol, glycol, polyethylene glycol, polypropylene glycol, polyvinyl alcohol, 2,6-di-(hydroxyethyl) pyridine, 2,4,6-tri-(hydroxyethyl) pyridine, tri-(hydroxymethyl) aminomethane, dimethylsilane diol, methylsilane triol, catechol, resorcinol, hydroquinone, pyrogallol, inositol, dihydroxynaphthol, thioglycol, and alizarine. Exemplified organometallics are diethyl and diisobutyl zinc, and tetraethyl tin. The catalyst is preferably formed in a hydrocarbon diluent such as benzene.
GB21047/62A 1961-06-02 1962-05-31 A method for preparing alkylene oxide polymers Expired GB983814A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1971361 1961-06-02

Publications (1)

Publication Number Publication Date
GB983814A true GB983814A (en) 1965-02-17

Family

ID=12006914

Family Applications (1)

Application Number Title Priority Date Filing Date
GB21047/62A Expired GB983814A (en) 1961-06-02 1962-05-31 A method for preparing alkylene oxide polymers

Country Status (2)

Country Link
FR (1) FR1324110A (en)
GB (1) GB983814A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3639267A (en) * 1969-12-19 1972-02-01 Hercules Inc Organozinc catalyst composition
EP0239973A2 (en) * 1986-03-31 1987-10-07 Union Carbide Corporation Catalyst and process for alkylene oxide polymerization
CN116082618A (en) * 2021-11-05 2023-05-09 万华化学集团股份有限公司 Preparation method of isopentenol polyoxyethylene ether

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3639267A (en) * 1969-12-19 1972-02-01 Hercules Inc Organozinc catalyst composition
EP0239973A2 (en) * 1986-03-31 1987-10-07 Union Carbide Corporation Catalyst and process for alkylene oxide polymerization
EP0239973A3 (en) * 1986-03-31 1989-11-08 Union Carbide Corporation Catalyst and process for alkylene oxide polymerization
CN116082618A (en) * 2021-11-05 2023-05-09 万华化学集团股份有限公司 Preparation method of isopentenol polyoxyethylene ether

Also Published As

Publication number Publication date
FR1324110A (en) 1963-04-12

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