[go: up one dir, main page]

GB310055A - - Google Patents

Info

Publication number
GB310055A
GB310055A GB1234129A GB1234129A GB310055A GB 310055 A GB310055 A GB 310055A GB 1234129 A GB1234129 A GB 1234129A GB 1234129 A GB1234129 A GB 1234129A GB 310055 A GB310055 A GB 310055A
Authority
GB
United Kingdom
Prior art keywords
molecular
phenol
heated
catalyst
catalysts
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
GB1234129A
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.)
Schering Kahlbaum AG
Original Assignee
Schering Kahlbaum AG
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 Schering Kahlbaum AG filed Critical Schering Kahlbaum AG
Publication of GB310055A publication Critical patent/GB310055A/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
    • C07C45/006Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by hydrogenation of aromatic hydroxy compounds

Landscapes

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

Abstract

310,055. Schering-Kahlbaum Akt.- Ges. April 21, 1928, [Convention date]. Ketones; alcohols. - Cyclic ketones are prepared by reacting with two molecular proportions of a cyclic alcohol on one molecular proportion of a phenol in the presence of a hydrogenation catalyst at about 200<0> C. In examples, (1) two molecular proportions of cyclohexanol are heated with one molecular proportion of phenol in the presence of a hydrogenating catalyst, cyclohexanone being obtained, (2) two molecular proportions of isoborneol are heated with one molecular proportion of phenol as above, the camphor being separated by centrifuging from cyclohexanone. The catalysts employed in the examples are nickel catalysts or mixed catalysts with nickel as a basis. The Specification as open to inspection under Sect. 91 (3) (a) describes the preparation of hydrogenated and dehydrogenated compounds by causing the interaction of a more or less completely hydrogenated compound with a compound capable of taking up hydrogen in the presence of a hydrogenation catalyst, and an example is given in which isoborneol is heated with carbon monoxide under pressure in the presence of a catalyst, giving methyl alcohol and camphor. This subject-matter does not appear in the Specification as accepted.
GB1234129A 1928-04-22 1929-04-20 Expired GB310055A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DESCH86206D DE669050C (en) 1928-04-22 1928-04-22 Process for making cyclic ketones

Publications (1)

Publication Number Publication Date
GB310055A true GB310055A (en) 1930-07-21

Family

ID=7443414

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1234129A Expired GB310055A (en) 1928-04-22 1929-04-20

Country Status (3)

Country Link
DE (1) DE669050C (en)
GB (1) GB310055A (en)
NL (1) NL25100C (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0822173A1 (en) * 1996-08-01 1998-02-04 Hoechst Celanese Corporation A new process for the manufacture of 1,3-cyclohexanedione
WO2009085826A2 (en) * 2007-12-20 2009-07-09 Si Group, Inc. Transhydrogenation processes

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE752239C (en) * 1939-05-07 1953-05-11 Ig Farbenindustrie Ag Process for the manufacture of cyclohexanone and its substitute products
DE1124487B (en) * 1959-05-15 1962-03-01 Stamicarbon Process for the production of cyclohexanone
DE1150070B (en) * 1959-12-14 1963-06-12 Scient Design Co Process for the production of pure cyclohexanone
BE598093A (en) * 1959-12-14 1961-03-31 Scient Design Co Process for the recovery of adipic acid precursors, such as cyclohexanol and cyclohexanone.
DE1233858B (en) * 1959-12-16 1967-02-09 Basf Ag Process for the production of pure cyclohexanone and cyclohexanol

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0822173A1 (en) * 1996-08-01 1998-02-04 Hoechst Celanese Corporation A new process for the manufacture of 1,3-cyclohexanedione
WO2009085826A2 (en) * 2007-12-20 2009-07-09 Si Group, Inc. Transhydrogenation processes
WO2009085826A3 (en) * 2007-12-20 2009-09-11 Si Group, Inc. Transhydrogenation processes

Also Published As

Publication number Publication date
DE669050C (en) 1938-12-15
NL25100C (en)

Similar Documents

Publication Publication Date Title
PAPA et al. Reductions with nickel-aluminum alloy and aqueous alkali
GB310055A (en)
JPS5918373B2 (en) Volatilization retention agent for fragrance compositions
Bailey et al. Pyrolysis of Esters. II. Direction of Elimination in Pyrolysis of Tertiary Esters1, 2
GB312345A (en) Improvements in catalytic dehydrogenation
GB449957A (en) Improvements in or relating to the hydrogenation of rubber
US2118954A (en) Hydrogenation of phenol-ketone
US3405185A (en) Production of isomenthol isomers
ES388905A1 (en) 2-2-disubstituted cycloalkane-1,3-diones
CH647494A5 (en) NEW FRAGRANCES.
GB1106088A (en) Process for the preparation of phloroglucinol
Nigam et al. Essential Oils and Their Constituents. XXI. 1 Isomerization of α-Humulene Monoxide to β-Humulen-7-ol. A New Sesquiterpene Alcohol
GB293001A (en) Process for the manufacture of hydrogenation products
US1771089A (en) Hans jordan
GB320638A (en) Process for the manufacture of alkylated phenols and their hydrogenation products
DE682294C (en) Process for the production of secondary, mixed aliphatic-cyclic alcohols
GB576680A (en) Improvements in the manufacture of cyclic aliphatic dihydroxy compounds
GB520201A (en) Method of hydrogenating ketones and aldehydes
DE711888C (en) Process for the refinement of synthetic resins
US1870071A (en) Production of piperidine
GB280924A (en) Process for the manufacture of thymol, its isomers or homologues and their hydrogenation products
GB344970A (en) Process for the manufacture of thymol and its isomers and homologues
US1704630A (en) Manufacture of menthol
GB338807A (en) Manufacture of 1:3-butylene-glycol by hydrogenising paraldol
UEDA Studies on the Reduction of Terpenes with Sodium in Aqueous Ammonia Part X. Synthesis of Menthol from Acetone and Formaldehyde