GB781765A - Process for the manufacture of alkylene oxide condensation products - Google Patents

Process for the manufacture of alkylene oxide condensation products

Info

Publication number
GB781765A
GB781765A GB13620/54A GB1362054A GB781765A GB 781765 A GB781765 A GB 781765A GB 13620/54 A GB13620/54 A GB 13620/54A GB 1362054 A GB1362054 A GB 1362054A GB 781765 A GB781765 A GB 781765A
Authority
GB
United Kingdom
Prior art keywords
reaction
ethylene oxide
reactor
liquid
oxide
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
GB13620/54A
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.)
BASF Schweiz AG
Original Assignee
Ciba 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 Ciba AG filed Critical Ciba AG
Publication of GB781765A publication Critical patent/GB781765A/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B61/00Other general methods

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)

Abstract

Alkylene oxide condensation products are prepared by reaction of alkylene oxides in the vaporized state with organic or inorganic compounds containing at least one reactive hydrogen atom and in the form of a finely-divided liquid or solution in a circulatory apparatus in which the liquid reaction mixture is continuously withdrawn and recycled to the reactor, the alkylene oxide being evaporated outside the reaction zone and then introduced into the reaction zone in the form of vapour under substantially atmospheric pressure for reaction with the finely-divided second reagent. Specified reagents are carboxylic acids, amides, amines, mercaptans, hydroxy-compounds and sodium bisulphite, and ethylene, propylene and butylene oxides, preferably used without a diluent. Temperatures of 50-200 DEG C. are suitable and catalysts may be present. Suitable apparatus is described. Examples illustrate the reaction of octyl phenol with about 8 mols. of ethylene oxide, castor oil with about 15 mols. of ethylene oxide and aqueous sodium bisulphite with about one mol. of ethylene oxide. Specification 683,884 is referred to.ALSO:Alkylene oxide condensation products are prepared by reaction of alkylene oxides in a vaporized state with organic or inorganic compounds containing at least one active hydrogen atom and in the form of a finely divided liquid or of a finely divided solution in a circulatory apparatus in which the liquid reaction mixture is continuously withdrawn and recycled to the reactor, the alkylene oxide being evaporated outside the reaction zone and then continuously introduced into the reaction zone in the form of vapour under substantially atmospheric pressure for reaction with the finely divided droplets of the second reagent. Specified reagents are ethylene, propylene and butylene oxides, which are preferably used without a diluent, and carboxylic acids, amides, amines, mercaptans, hydroxy-compounds including alkyl-phenols and sodium bisulphite. Reaction temperatures of 50-200 DEG C. are suitable. Catalysts may be present. According to examples using illustrated apparatus (not shown) : (1) octyl-phenol containing added sodium as catalyst is heated in a vented cylindrical reactor to 150 DEG C. and the liquid phenol is continuously cycled by a pump from the base of the reactor to a centrifugal nozzle at the top; liquid ethylene oxide is fed to an evaporator and the vaporized oxide is then passed continuously into the top of the reactor at atmospheric pressure at a rate such that substantially no ethylene oxide gas escapes from the reactor vent; about 8 mols. of ethylene oxide are combined with 1 mol. of phenol; in like manner (2) castor oil is reacted with about 15 molar proportions of ethylene oxide; and (3) sodium bisulphite in aqueous solution with about one molar proportion of ethylene oxide. Specification 683,884 is referred to.
GB13620/54A 1953-05-13 1954-05-10 Process for the manufacture of alkylene oxide condensation products Expired GB781765A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH781765X 1953-05-13

Publications (1)

Publication Number Publication Date
GB781765A true GB781765A (en) 1957-08-28

Family

ID=4536286

Family Applications (1)

Application Number Title Priority Date Filing Date
GB13620/54A Expired GB781765A (en) 1953-05-13 1954-05-10 Process for the manufacture of alkylene oxide condensation products

Country Status (1)

Country Link
GB (1) GB781765A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3102893A (en) * 1959-09-30 1963-09-03 Monsanto Chemicals Polyether-substituted glycidyl ethers
US4385173A (en) 1980-04-21 1983-05-24 Shell Oil Company Polyol polyether preparation process

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3102893A (en) * 1959-09-30 1963-09-03 Monsanto Chemicals Polyether-substituted glycidyl ethers
US4385173A (en) 1980-04-21 1983-05-24 Shell Oil Company Polyol polyether preparation process

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