GB400384A - Improvements relating to the production of higher ketones - Google Patents

Improvements relating to the production of higher ketones

Info

Publication number
GB400384A
GB400384A GB2283232A GB2283232A GB400384A GB 400384 A GB400384 A GB 400384A GB 2283232 A GB2283232 A GB 2283232A GB 2283232 A GB2283232 A GB 2283232A GB 400384 A GB400384 A GB 400384A
Authority
GB
United Kingdom
Prior art keywords
mols
alcohol
ketone
oxide
copper
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
GB2283232A
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.)
Evonik Operations GmbH
Original Assignee
Degussa GmbH
Deutsche Gold und Silber Scheideanstalt
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 Degussa GmbH, Deutsche Gold und Silber Scheideanstalt filed Critical Degussa GmbH
Priority to GB2283232A priority Critical patent/GB400384A/en
Publication of GB400384A publication Critical patent/GB400384A/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
    • C07C45/70Preparation 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 with functional groups containing oxygen only in singly bound form
    • C07C45/71Preparation 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 with functional groups containing oxygen only in singly bound form being hydroxy groups

Abstract

Catalysts for the conversion of lower into higher aliphatic ketones with the aid of lower aliphatic primary alcohols consist of aluminium xide with or without magnesia or other alkaline earth metal oxide as main constituent with relatively small amounts of copper and/or silver or an oxide thereof, to which molybdenum trioxide may be added. The catalysts used in the examples are prepared by (1) impregnating alumina with copper formate and molybdenum trioxide or barium oxide, (2) spreading magnesium oxide and aluminium hydroxide with small quantities of copper and silver oxides, (3) impregnating alumina with copper formate, (4) mixing magnesium oxide with aluminium hydroxide and copper oxide; in each case, the product is heated with air and steam. Specifications 326,812, [Class 1 (i), Chemical processes &c.], and 364,134 are referred to.ALSO:Higher aliphatic ketones are prepared by subjecting a mixture of a lower aliphatic ketone with a lower aliphatic primary alcohol together with hydrogen or nitrogen to a temperature of 150-400 DEG C. in the presence of a catalyst consisting of aluminium oxide with or without magnesia or other alkaline-earth metal oxide as main constituent with relatively small amounts of copper and/or silver or an oxide thereof, to which molybdenum trioxide may be added. The reaction may be effected discontinuously in an autoclave, or by continuously passing the reactants over the catalyst at ordinary or increased pressure. Both the hydrogen and nitrogen are stated to act primarily as diluents, but when using hydrogen small amounts of higher primary alcohols are also formed. According to the examples, (1) methyl alcohol and acetone in equimolecular quantities are passed with at least an equal volume of nitrogen over a catalyst prepared by impregnating alumina with copper formate and molybdenum trioxide or barium oxide and treating with air and steam at 450 DEG C.; the product contains methylethyl ketone, diethyl ketone and high-boiling polysubstituted ketones; (2) a mixture of acetone (1,25 mols.), ethyl alcohol (1 mol.), and hydrogen (1,5 mols.) is passed over a catalyst prepared by kneading magnesium oxide and aluminium hydroxide with small quantities of copper and silver oxides and heating the mixture with air and steam; methylpropyl ketone, dipropyl ketone and high-boiling ketones are obtained, together with butyl and hexyl alcohol; an alternative catalyst is prepared by impregnating alumina with copper formate; (3) magnesium oxide is mixed with aluminium hydroxide and copper oxide and treated with air and steam at 400-500 DEG C., and over this catalyst is passed a mixture of acetone (3,0 mols.), ethyl alcohol (2,5 mols.) and hydrogen (3.2 mols.) under pressure; the products comprise methylpropyl ketone and dipropyl ketone, together with butyl alcohol, hexyl alcohol and higher alcohols (4) a mixture of acetone (2,5 mols.), butyl alcohol (2 mols.) and hydrogen (3 mols.) is passed under pressure over the catalyst used in (3); methylamyl ketone is the principal product, but heptyl alcohol, octyl alcohol and higher ketones and alcohols are also formed; (5) methylethyl ketone (2 mols.), ethyl alcohol (3 mols.) and hydrogen (3 mols.) are passed under pressure over the catalyst used in (3), giving rise to higher ketones, mainly C6 and C8, together with butyl alcohol, hexyl alcohol and higher alcohols; (6) higher ketones, mainly methylamyl ketone, result from the heat treatment of butanol and acetone with hydrogen in an autoclave in the presence of the catalyst employed in (3). Specifications 326,812, [Class 2 (iii), Dyes &c.], and 364,134 are referred to. The Specification as open to inspection under Sect. 91 describes the formation of higher ketones by catalytic interaction of a lower ketone with an aliphatic alcohol, in the presence or absence of a diluent gas. This subject-matter does not appear in the Specification as accepted.
GB2283232A 1932-08-15 1932-08-15 Improvements relating to the production of higher ketones Expired GB400384A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2283232A GB400384A (en) 1932-08-15 1932-08-15 Improvements relating to the production of higher ketones

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2283232A GB400384A (en) 1932-08-15 1932-08-15 Improvements relating to the production of higher ketones

Publications (1)

Publication Number Publication Date
GB400384A true GB400384A (en) 1933-10-26

Family

ID=10185764

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2283232A Expired GB400384A (en) 1932-08-15 1932-08-15 Improvements relating to the production of higher ketones

Country Status (1)

Country Link
GB (1) GB400384A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2549508A (en) * 1948-10-15 1951-04-17 Standard Oil Dev Co Preparation of unsaturated ketones and aldehydes
WO2014176552A3 (en) * 2013-04-26 2015-01-08 The Regents Of The University Of California Methods to produce fuels
US9856427B2 (en) 2011-05-27 2018-01-02 The Regents Of The University Of California Method to convert fermentation mixture into fuels
US10106480B2 (en) 2014-10-29 2018-10-23 The Regents Of The University Of California Methods for producing fuels, gasoline additives, and lubricants using amine catalysts
US10138193B2 (en) 2014-10-29 2018-11-27 The Regents Of The University Of California Methods for producing fuels, gasoline additives, and lubricants using amine catalysts
US10207961B2 (en) 2014-03-24 2019-02-19 The Regents Of The University Of California Methods for producing cyclic and acyclic ketones

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2549508A (en) * 1948-10-15 1951-04-17 Standard Oil Dev Co Preparation of unsaturated ketones and aldehydes
US9856427B2 (en) 2011-05-27 2018-01-02 The Regents Of The University Of California Method to convert fermentation mixture into fuels
WO2014176552A3 (en) * 2013-04-26 2015-01-08 The Regents Of The University Of California Methods to produce fuels
CN105308015A (en) * 2013-04-26 2016-02-03 加利福尼亚大学董事会 Methods to produce fuels
US9790444B2 (en) 2013-04-26 2017-10-17 The Regents Of The University Of California Methods to produce fuels
EA032556B1 (en) * 2013-04-26 2019-06-28 Дзе Риджентс Оф Дзе Юниверсити Оф Калифорния Methods to produce fuels
US10207961B2 (en) 2014-03-24 2019-02-19 The Regents Of The University Of California Methods for producing cyclic and acyclic ketones
US10618856B2 (en) 2014-03-24 2020-04-14 The Regents Of The University Of California Methods for producing cyclic and acyclic ketones
US10106480B2 (en) 2014-10-29 2018-10-23 The Regents Of The University Of California Methods for producing fuels, gasoline additives, and lubricants using amine catalysts
US10138193B2 (en) 2014-10-29 2018-11-27 The Regents Of The University Of California Methods for producing fuels, gasoline additives, and lubricants using amine catalysts

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