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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/45—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
- C07C45/48—Preparation 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.
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)
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)
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 |
-
1963
- 1963-05-28 CH CH667163A patent/CH425752A/en unknown
- 1963-05-29 AT AT433763A patent/AT242689B/en active
- 1963-05-31 GB GB2201163A patent/GB1030003A/en not_active Expired
- 1963-05-31 BE BE633124A patent/BE633124A/en unknown
- 1963-06-07 ES ES288832A patent/ES288832A1/en not_active Expired
- 1963-06-07 DK DK269463A patent/DK105269C/en active
Cited By (2)
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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