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GB434104A - Improvements in or relating to the manufacture of organic condensation products - Google Patents

Improvements in or relating to the manufacture of organic condensation products

Info

Publication number
GB434104A
GB434104A GB3291133A GB3291133A GB434104A GB 434104 A GB434104 A GB 434104A GB 3291133 A GB3291133 A GB 3291133A GB 3291133 A GB3291133 A GB 3291133A GB 434104 A GB434104 A GB 434104A
Authority
GB
United Kingdom
Prior art keywords
oxide
oxides
condensation products
catalyst
alcohols
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
GB3291133A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Priority to GB3291133A priority Critical patent/GB434104A/en
Publication of GB434104A publication Critical patent/GB434104A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/67Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C07C45/68Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C45/72Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
    • C07C45/73Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups combined with hydrogenation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/002Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by dehydrogenation

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)

Abstract

Condensation products of higher molecular weight, such as ketones, alcohols and hydrocarbons are obtained by treating a secondary alcohol with a dehydrogenating catalyst at temperatures from 200--500 DEG C. and pressures of from 2--750 atmospheres, the yield of condensation products such as higher alcohols increasing with the pressure. The process may be carried out either in the liquid or in the vapour phase. Suitable catalysts include difficultly reducible oxides, such as zinc oxide, manganese oxide or magnesium oxide or mixtures thereof or with other oxides which may be less active but more acidic than the above oxides, e.g. oxides of vanadium, tungsten, molybdenum or uranium which act as promoters. Preferably the catalyst contains one or more components having dehydrogenating characteristics and one or more dehydrating metal oxides, e.g. chromium oxide, aluminium oxide or thorium oxide. A preferred catalyst consists of chromium oxide and manganese oxide or zinc oxide. Preferably, the dehydrogenating components are in the combined state, e.g. as oxide or in the form of a compound with the dehydrating oxide. Suitable catalysts of this type are described in Specifications 272,555, 301,806, and 313,575, [all in Class 2 (iii)]. Examples of secondary alcohols which may be treated are isopropanol, secondary butanol, diethyl carbinol, methyl normal propyl carbinol, and methyl isopropyl carbinol. According to examples (1) isopropanol vapour is passed over a zinc-copper-cadmium chromite catalyst at a temperature of 390 DEG C. and a pressure of 200 atmospheres. The condensate contains acetone, low boiling hydrocarbons, higher alcohols and ketones and other higher condensation products; (2) secondary butyl alcohol is vaporized and passed over a zinc-copper-cadmium chromite catalyst at 350 DEG C. and 200 atmospheres pressure. The condensate contains higher products as in the above example in addition to methyl ethyl ketone. If the reaction is carried out under atmospheric pressure, low boiling ketones are chiefly obtained, free from condensation products.ALSO:Condensation products of higher molecular weight, such as ketones, alcohols and hydrocarbons, are obtained by treating a secondary alcohol with a dehydrogenating catalyst at temperatures from 200--500 DEG C. and pressures of from 2--750 atmospheres, the yield of condensation products such as higher alcohols increasing with the pressure. The process may be carried out either in the liquid or in the vapour phase. Suitable catalysts include difficulty reducible oxides such as zinc oxide, manganese oxide or magnesium oxide or mixtures thereof or with other oxides which may be less active but more acidic than the above oxides, e.g. oxides of vanadium, tungsten, molybdenum or uranium which act as promoters. Preferably the catalyst contains one or more components having dehydrogenating characteristics and one or more dehydrating metal oxides, e.g. chromium oxide, aluminium oxide or thorium oxide. A preferred catalyst consists of chromium oxide and manganese oxide or zinc oxide. Preferably the dehydrogenating components are in the combined state, e.g. as oxide or in the form of a compound with the dehydrating oxide. Suitable catalysts of this type are described in Specifications 272,555, 301,806, and 313,575, [all in Class 1 (i)]. Examples of secondary alcohols which may be treated are isopropanol, secondary butanol, diethyl carbinol, methyl normal propyl carbinol and methyl isopropyl carbinol. According to examples, isopropanol and secondary butyl alcohol are treated in the vapour phase in the presence of a zinc-copper-cadmium chromite catalyst at 200 atmospheres pressure and temperatures of 390 and 350 DEG C. respectively. The products are low boiling hydrocarbons, higher alcohols and ketones and other higher condensation products, in addition to acetone and methyl-ethyl ketone. If the reaction is carried out at atmospheric pressure, low-boiling ketones are chiefly obtained, free from condensation products.
GB3291133A 1933-11-24 1933-11-24 Improvements in or relating to the manufacture of organic condensation products Expired GB434104A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3291133A GB434104A (en) 1933-11-24 1933-11-24 Improvements in or relating to the manufacture of organic condensation products

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3291133A GB434104A (en) 1933-11-24 1933-11-24 Improvements in or relating to the manufacture of organic condensation products

Publications (1)

Publication Number Publication Date
GB434104A true GB434104A (en) 1935-08-26

Family

ID=10345840

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3291133A Expired GB434104A (en) 1933-11-24 1933-11-24 Improvements in or relating to the manufacture of organic condensation products

Country Status (1)

Country Link
GB (1) GB434104A (en)

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