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GB1030003A - - Google Patents

Info

Publication number
GB1030003A
GB1030003A GB2201163A GB2201163A GB1030003A GB 1030003 A GB1030003 A GB 1030003A GB 2201163 A GB2201163 A GB 2201163A GB 2201163 A GB2201163 A GB 2201163A GB 1030003 A GB1030003 A GB 1030003A
Authority
GB
United Kingdom
Prior art keywords
acids
oxide
catalyst
present
mixture
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
GB2201163A
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.)
SNIA Viscosa SpA
Original Assignee
SNIA Viscosa SpA
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 SNIA Viscosa SpA filed Critical SNIA Viscosa SpA
Publication of GB1030003A publication Critical patent/GB1030003A/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
    • C07C45/45Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
    • C07C45/48Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation involving decarboxylation

Landscapes

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

Abstract

Cyclohexyl phenyl ketone is made by reacting a mixture of benzene and hexahydrobenzoic acids at 280 DEG to 480 DEG C. in the presence of a catalyst comprising the manganous salts of the said acids. The catalyst is made by dissolving manganous oxide, or manganese carbonate, in a mixture of the acids. Preferably for 2 moles of acids there are present 1.1 to 1.3 mols. of manganous oxide. The catalyst may also be made by double decomposition from the two acids and appropriate manganese salts. Other metal oxides, e.g. magnesium or lithium oxide, may be present and, if so, an additional amount of the acids, equivalent to the quantity of inert oxide, should also be present. Preferably there is an excess of 0.1-0.3 moles of hexahydrobenzoic acid in relation to the benzoic acid. Preferred temperatures are 330 DEG to 370 DEG C. Activity of the catalyst may be maintained by passing steam through the reaction mixture. Oxidation of the catalyst is prevented by passing small quantities of hydrogen through the reaction mixture. Sub-, normal- or elevated-pressures may be adopted. Examples are provided.ALSO:A catalyst containing manganese, in the manganous form, is made by dissolving manganese oxide, or carbonate, in a mixture of hexahydrobenzoic and benzoic acids or by double decomposition from the acid mixture and appropriate manganese salts. Preferably for each two moles of acid mixture there are present 1.1 to 1.3 moles of manganous oxide. Inert oxides e.g. magnesium and lithium oxides, may be present and if so, an additional quantity of the acids, equivalent to the amount of inert oxide, should also be present. Catalytic activity may be maintained by effecting the reaction in the presence of steam and/or hydrogen.
GB2201163A 1962-05-07 1963-05-31 Expired GB1030003A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IT1125662 1962-05-07

Publications (1)

Publication Number Publication Date
GB1030003A true GB1030003A (en) 1966-05-18

Family

ID=11134839

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2201163A Expired GB1030003A (en) 1962-05-07 1963-05-31

Country Status (6)

Country Link
AT (1) AT242689B (en)
BE (1) BE633124A (en)
CH (1) CH425752A (en)
DK (1) DK105269C (en)
ES (1) ES288832A1 (en)
GB (1) GB1030003A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6881865B2 (en) 2002-09-27 2005-04-19 Korea Kumho Petrochemical Co., Ltd. Method for preparing cyclohexyl phenyl ketone from 1,3-butadiene and acrylic acid
CN112439410A (en) * 2020-12-03 2021-03-05 长沙新宇高分子科技有限公司 Catalyst for synthesizing aromatic ketone and method for catalytically synthesizing aromatic ketone by using same

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1233861B (en) * 1963-04-06 1967-02-09 Edison Soc Process for the preparation of cycloalkylaryl ketones

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6881865B2 (en) 2002-09-27 2005-04-19 Korea Kumho Petrochemical Co., Ltd. Method for preparing cyclohexyl phenyl ketone from 1,3-butadiene and acrylic acid
CN112439410A (en) * 2020-12-03 2021-03-05 长沙新宇高分子科技有限公司 Catalyst for synthesizing aromatic ketone and method for catalytically synthesizing aromatic ketone by using same

Also Published As

Publication number Publication date
BE633124A (en) 1963-12-02
ES288832A1 (en) 1963-08-01
AT242689B (en) 1965-09-27
DK105269C (en) 1966-09-12
CH425752A (en) 1966-12-15

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