GB886157A - Process for the manufacture of aldehydes or ketones - Google Patents

Process for the manufacture of aldehydes or ketones

Info

Publication number
GB886157A
GB886157A GB18432/58A GB1843258A GB886157A GB 886157 A GB886157 A GB 886157A GB 18432/58 A GB18432/58 A GB 18432/58A GB 1843258 A GB1843258 A GB 1843258A GB 886157 A GB886157 A GB 886157A
Authority
GB
United Kingdom
Prior art keywords
aqueous solution
spray
solution
ketone
tower
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
GB18432/58A
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.)
Consortium fuer Elektrochemische Industrie GmbH
Original Assignee
Consortium fuer Elektrochemische Industrie GmbH
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 Consortium fuer Elektrochemische Industrie GmbH filed Critical Consortium fuer Elektrochemische Industrie GmbH
Publication of GB886157A publication Critical patent/GB886157A/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
    • C07C45/27Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/30Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with halogen containing compounds, e.g. hypohalogenation
    • 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
    • C07C45/27Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/28Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of CHx-moieties

Landscapes

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

Abstract

Aldehydes and ketones are produced by contacting hydrocarbons which contain olefinic bonds with an aqueous solution of a compound of a metal of the platinum group at a temperature in the range 0 DEG C.-250 DEG C., whereby an aldehyde or ketone having the same number of carbon atoms as the initial hydrocarbon is obtained. Suitable metallic compounds are: palladium chloride, hexachloroplatinic acid, rhodium chloride, and palladium phosphate. The aqueous solution preferably contains free hydrochloric, sulphuric or phosphoric acid. The hydrocarbon may be brought into intimate contact with the aqueous solution by means of a spray-tower, packed column, or stirring-vessel. In order to increase the miscibility, a solvent, such as glacial acetic acid or dioxane, may be added. In Example (1), propylene is irrigated in a spray-tower at 80 DEG C. under a pressure of 80 atm. with an aqueous solution which contains 17.8 grm. PdCl2 and 55 grm. HCl per litre. The effluent solution is distilled in a column; and acetone is obtained as distillate. The aqueous solution, which now contains precipitated palladium, is pumped from the still to a second spray-tower, in which it is contacted with oxygen at 80 DEG C. and a pressure of 50 atm. The clear solution so obtained is re-used for irrigating propylene. The velocity of circulation of the solution is adjusted so that the solution remains in the spray-towers for 15 minutes. Examples 5 and 8 relate to the preparation of acetaldehyde by the action of an aqueous solution of palladium chloride and of rhodium chloride, respectively, on ethylene. Example 6 relates to the production of acetophenone from styrene. Examples 3, 7 and 9 relate to the production of n-octyl-methyl ketone, benzyl-methyl-ketone, cyclopentanone, b -indanone, pentene-2-al-1, crotonaldehyde, cyclohexanone, and methyl-ethyl ketone.
GB18432/58A 1957-06-07 1958-06-09 Process for the manufacture of aldehydes or ketones Expired GB886157A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE886157X 1957-06-07

Publications (1)

Publication Number Publication Date
GB886157A true GB886157A (en) 1962-01-03

Family

ID=6833169

Family Applications (1)

Application Number Title Priority Date Filing Date
GB18432/58A Expired GB886157A (en) 1957-06-07 1958-06-09 Process for the manufacture of aldehydes or ketones

Country Status (1)

Country Link
GB (1) GB886157A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3333004A (en) * 1962-07-18 1967-07-25 Basf Ag Production of glyoxal
US3668257A (en) * 1966-08-08 1972-06-06 Union Oil Co Oxidation of olefins
EP0457387A2 (en) * 1990-05-14 1991-11-21 Shell Internationale Researchmaatschappij B.V. Process for the preparation of ketones

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3333004A (en) * 1962-07-18 1967-07-25 Basf Ag Production of glyoxal
US3668257A (en) * 1966-08-08 1972-06-06 Union Oil Co Oxidation of olefins
EP0457387A2 (en) * 1990-05-14 1991-11-21 Shell Internationale Researchmaatschappij B.V. Process for the preparation of ketones
EP0457387A3 (en) * 1990-05-14 1992-04-15 Shell Internationale Research Maatschappij B.V. Process for the preparation of ketones

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