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GB745946A - Improvements in the production of saturated ketones - Google Patents

Improvements in the production of saturated ketones

Info

Publication number
GB745946A
GB745946A GB2199553A GB2199553A GB745946A GB 745946 A GB745946 A GB 745946A GB 2199553 A GB2199553 A GB 2199553A GB 2199553 A GB2199553 A GB 2199553A GB 745946 A GB745946 A GB 745946A
Authority
GB
United Kingdom
Prior art keywords
chromium
acid
activated
copper
hydrogenation
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
GB2199553A
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to GB2199553A priority Critical patent/GB745946A/en
Publication of GB745946A publication Critical patent/GB745946A/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
    • C07C45/65Preparation 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 splitting-off hydrogen atoms or functional groups; by hydrogenolysis of functional groups
    • 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
    • C07C45/65Preparation 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 splitting-off hydrogen atoms or functional groups; by hydrogenolysis of functional groups
    • C07C45/66Preparation 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 splitting-off hydrogen atoms or functional groups; by hydrogenolysis of functional groups by dehydration
    • 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
    • C07C45/673Preparation 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 change of size of the carbon skeleton
    • 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

Landscapes

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

Abstract

A process for the production of saturated ketones comprises hydrogenating a ketol, preferably one with a tertiary hydroxyl group, in the presence of a hydrogenation catalyst and a free acid which remains a free acid in the presence of hydrogen at elevated temperature. Suitable catalysts are metals of the first or eighth sub group of the periodic system which may be activated by chromium, alkali metals, magnesium, boron or alumina and may be deposited on a carrier such as pumice, silica gel, kieselguhr, charcoal, coke, chamotte or porcelain. Non-volatile acids derived from phosphorus or boron, such as phosphoric, boric, phosphomolybdic, phosphotungstic and borotungstic acids or borylphosphate are preferred, but volatile organic acids such as formic, acetic and propionic acids and aromatic acids such as benzoic, phenylacetic and phthalic acids are also suitable. The carrier-free hydrogenation catalyst may be added to the ketol in which at least 5 per cent of an organic acid is dissolved, or the catalyst or the inorganic acid may be suspended on a carrier. Hydrogenation at high pressure, e.g. 100 to 300 atmospheres, is preferred. The process may be effected intermittently or batchwise. Temperatures of about 150 DEG to 300 DEG C. are suitable. Ketols obtainable by condensation with aqueous alkali hydroxides such as pentanolone-2,4, diacetone alcohol), 3-methyl-pentanolone-2,4, heptanolone-2,4, undecanolone-2,4, benzoylisopropanol and (1-hydroxypropyl)-cyclohexanone can be hydrogenated. In examples diacetone alcohol is hydrogenated (1) in an autoclave with acetic acid and a chromium-activated to give acetone, isopropanol, hexone, methylpentanol and components of higher boiling-point; (2) as in (1), in the presence of added water, to give hexone and cleavage products; (3) by passage with hydrogen under pressure through a heated tube containing a catalyst comprising copper and chromium with phosphoric acid on silica gel, to give acetone, isopropanol, hexone and mesityl oxide; (4) by passage with hydrogen through a heated tube containing boric acid, phosphoric acid, copper, nickel and chromium (obtained by mixing borylphosphate and a CuNi-hydrogenation catalyst, activated with chromium) to give acetone, isopropanol, methyl pentanone and hexone; (5) by passage under pressure with hydrogen through a heated tube charged with a mixture of coke, phosphoric acid, Na2H2P2O7, trimetaphosphate and Madrell salt and a hydrogenation catalyst containing cooper, nickel, chromium and kieselguhr to give hexone and higher-boiling materials.ALSO:As hydrogenation catalysts for use in a process of preparing a saturated ketone by hydrogenation of a ketol in the presence of a free acid which remains a free acid in the presence of hydrogen at elevated temperature (see Group IV(b)), there are specified metals of the first or eighth group of the periodic system which may be activated by chromium, alkali metals, magnesium, boron or alumina and may be deposited on a carrier such as pumice, silica gel, kieselguhr, charcoal, coke, chamotte or porcelain. In examples there are employed (1) and (2) a carrier-free copper catalyst activated by chromium, (3) a catalyst containing copper, phosphoric acid, chromium and silica gel, (4) a mixture of boric acid, phosphoric acid, copper, nickel, chromium and kieselguhr obtained by mixing boryl phosphate and a Cu-Ni-hydrogenation catalyst activated with chromium (5) a mixture of coke phosphoric acid Na2H2P2O7, trimetaphosphate and Madrell salt and a hydrogenation catalyst containing copper, nickel, chromium and kieselguhr.
GB2199553A 1953-08-10 1953-08-10 Improvements in the production of saturated ketones Expired GB745946A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2199553A GB745946A (en) 1953-08-10 1953-08-10 Improvements in the production of saturated ketones

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2199553A GB745946A (en) 1953-08-10 1953-08-10 Improvements in the production of saturated ketones

Publications (1)

Publication Number Publication Date
GB745946A true GB745946A (en) 1956-03-07

Family

ID=10172228

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2199553A Expired GB745946A (en) 1953-08-10 1953-08-10 Improvements in the production of saturated ketones

Country Status (1)

Country Link
GB (1) GB745946A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0276767A2 (en) * 1987-01-28 1988-08-03 BASF Aktiengesellschaft Process for the preparation of ketones
WO2012039839A1 (en) * 2010-09-23 2012-03-29 Celanese International Corporation Production of alcohols
CN102548944A (en) * 2009-10-09 2012-07-04 花王株式会社 Process for producing 2-alkylcycloalkanone
US8460405B2 (en) 2010-02-02 2013-06-11 Celanese International Corporation Ethanol compositions
US8541633B2 (en) 2010-02-02 2013-09-24 Celanese International Corporation Processes for producing anhydrous ethanol compositions
US8668750B2 (en) 2010-02-02 2014-03-11 Celanese International Corporation Denatured fuel ethanol compositions for blending with gasoline or diesel fuel for use as motor fuels
US8728179B2 (en) 2010-02-02 2014-05-20 Celanese International Corporation Ethanol compositions
US8747492B2 (en) 2010-02-02 2014-06-10 Celanese International Corporation Ethanol/fuel blends for use as motor fuels
US8932372B2 (en) 2010-02-02 2015-01-13 Celanese International Corporation Integrated process for producing alcohols from a mixed acid feed

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0276767A2 (en) * 1987-01-28 1988-08-03 BASF Aktiengesellschaft Process for the preparation of ketones
EP0276767A3 (en) * 1987-01-28 1988-10-05 Basf Aktiengesellschaft Process for the preparation of ketones
US4866210A (en) * 1987-01-28 1989-09-12 Basf Aktiengesellschaft Preparation of ketones
CN102548944B (en) * 2009-10-09 2014-12-10 花王株式会社 Process for producing 2-alkylcycloalkanone
CN102548944A (en) * 2009-10-09 2012-07-04 花王株式会社 Process for producing 2-alkylcycloalkanone
EP2487150A1 (en) * 2009-10-09 2012-08-15 Kao Corporation Process for producing 2-alkylcycloalkanone
EP2487150A4 (en) * 2009-10-09 2013-03-20 Kao Corp Process for producing 2-alkylcycloalkanone
US8541633B2 (en) 2010-02-02 2013-09-24 Celanese International Corporation Processes for producing anhydrous ethanol compositions
US8460405B2 (en) 2010-02-02 2013-06-11 Celanese International Corporation Ethanol compositions
US8668750B2 (en) 2010-02-02 2014-03-11 Celanese International Corporation Denatured fuel ethanol compositions for blending with gasoline or diesel fuel for use as motor fuels
US8728179B2 (en) 2010-02-02 2014-05-20 Celanese International Corporation Ethanol compositions
US8747492B2 (en) 2010-02-02 2014-06-10 Celanese International Corporation Ethanol/fuel blends for use as motor fuels
US8747493B2 (en) 2010-02-02 2014-06-10 Celanese International Corporation Ethanol compositions
US8858659B2 (en) 2010-02-02 2014-10-14 Celanese International Corporation Processes for producing denatured ethanol
US8932372B2 (en) 2010-02-02 2015-01-13 Celanese International Corporation Integrated process for producing alcohols from a mixed acid feed
US9447005B2 (en) 2010-02-02 2016-09-20 Celanese International Corporation Processes for producing anhydrous ethanol compositions
WO2012039839A1 (en) * 2010-09-23 2012-03-29 Celanese International Corporation Production of alcohols

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