GB1234766A - Vapour phase oxidation of diols - Google Patents

Vapour phase oxidation of diols

Info

Publication number
GB1234766A
GB1234766A GB4218067A GB4218067A GB1234766A GB 1234766 A GB1234766 A GB 1234766A GB 4218067 A GB4218067 A GB 4218067A GB 4218067 A GB4218067 A GB 4218067A GB 1234766 A GB1234766 A GB 1234766A
Authority
GB
United Kingdom
Prior art keywords
less
diol
surface area
gaseous mixture
catalyst
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
GB4218067A
Inventor
Brian Keith Howe
Robert Frederick Hardy
Douglas Alfred Clarke
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.)
Evonik LCL Ltd
Original Assignee
Laporte Chemicals Ltd
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 Laporte Chemicals Ltd filed Critical Laporte Chemicals Ltd
Priority to GB4218067A priority Critical patent/GB1234766A/en
Publication of GB1234766A publication Critical patent/GB1234766A/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
    • C07C45/32Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
    • C07C45/37Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of >C—O—functional groups to >C=O groups
    • C07C45/39Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of >C—O—functional groups to >C=O groups being a secondary hydroxyl group
    • 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
    • C07C45/32Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
    • C07C45/37Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of >C—O—functional groups to >C=O groups
    • C07C45/38Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of >C—O—functional groups to >C=O groups being a primary hydroxyl group

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

1,234,766. Vapcur phase oxidation of 1,2- diols. LAPORTE CHEMICALS Ltd. 12 Dec., 1968 [15 Sept., 1967], No. 42180/67. Heading C2C. A hydroxycarbonyl compound is obtained by contacting a gaseous mixture containing a 1,2- diol of the general formula RCH(OH)CH 2 OH, wherein R is H, methyl, ethyl, n-propyl or isopropyl group with molecular oxygen, the molar ratio of oxygen to the diol in the gaseous mixture being less than 4: 1 in the presence of a metallic copper, silver or gold catalyst having a surface area of less than 50 square metres per gram. The gaseous mixture preferably contains a diluent gas, e.g. nitrogen, CO 2 , argon or helium and water vapour should also desirably be present. The reaction temperature may be between the b.pt. of the diol and about 500‹ C., e.g. between 250‹ and 350‹ C. Examples are given for the oxidation of ethylene glycol to form glycollic aldehyde together with some glyoxal and a small amount of glycollic acid, the catalyst being either pure copper gauze spirals of surface area of less than 5 m.<SP>2</SP>/g. or a metallic silver catalyst in the form of spirals of surface area less than 5 m.<SP>2</SP>/g. When R is methyl the products are acetol and 2-hydroxy propionaldehyde.
GB4218067A 1967-09-15 1967-09-15 Vapour phase oxidation of diols Expired GB1234766A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB4218067A GB1234766A (en) 1967-09-15 1967-09-15 Vapour phase oxidation of diols

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4218067A GB1234766A (en) 1967-09-15 1967-09-15 Vapour phase oxidation of diols

Publications (1)

Publication Number Publication Date
GB1234766A true GB1234766A (en) 1971-06-09

Family

ID=10423197

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4218067A Expired GB1234766A (en) 1967-09-15 1967-09-15 Vapour phase oxidation of diols

Country Status (1)

Country Link
GB (1) GB1234766A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4511739A (en) * 1979-06-02 1985-04-16 Basf Aktiengesellschaft Continuous preparation of glyoxal
EP0217280A1 (en) * 1985-10-04 1987-04-08 Hoechst Aktiengesellschaft Process for the production of hydroxycarbonyl compounds from 1,2-diols
WO2007132011A1 (en) * 2006-05-17 2007-11-22 Basf Aktiengesellschaft Method for producing vicinal dioxo compounds by oxidation of vicinal dihydroxy compounds on a structured catalyst packing
CN103772169A (en) * 2014-02-12 2014-05-07 复旦大学 Method for synthesizing low-impurity content glyoxal through gas phase oxidation

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4511739A (en) * 1979-06-02 1985-04-16 Basf Aktiengesellschaft Continuous preparation of glyoxal
EP0217280A1 (en) * 1985-10-04 1987-04-08 Hoechst Aktiengesellschaft Process for the production of hydroxycarbonyl compounds from 1,2-diols
WO2007132011A1 (en) * 2006-05-17 2007-11-22 Basf Aktiengesellschaft Method for producing vicinal dioxo compounds by oxidation of vicinal dihydroxy compounds on a structured catalyst packing
CN103772169A (en) * 2014-02-12 2014-05-07 复旦大学 Method for synthesizing low-impurity content glyoxal through gas phase oxidation
CN103772169B (en) * 2014-02-12 2015-12-02 复旦大学 The low assorted content oxalic dialdehyde of a kind of gaseous oxidation synthesis method

Similar Documents

Publication Publication Date Title
Iwasawa et al. Reaction mechanism for styrene synthesis over polynaphthoquinone
JPS5295609A (en) Preparation of methacrylic acid
GB1374644A (en) Process for producing alpha,beta-unsaturated ketones and alcohols from bicyclic dompounds
GB1234766A (en) Vapour phase oxidation of diols
US3848010A (en) Catalytic vinylation of aromatic compounds
Bonner et al. The cool flame combustion of hydrocarbons II—Propane and n-heptane
US3804902A (en) Process for producing acetone
US2246569A (en) Process for oxidizing ethers
JPS5273810A (en) Production of glycol monoethers
KR920014756A (en) Method for producing methacrylic acid by catalytic oxidation of isobutane
JPS6287545A (en) Manufacture of hydroxycarbonyl compound from 1,2-diol
US4052442A (en) Process for preparing glycol esters
US3384669A (en) Process and catalyst for oxidizing olefins to carbonyl compounds
McCaffrey et al. The effect of the oxygen content in a series of manganese oxide catalysts on their catalytic activity and selectivity in the decomposition of isopropyl alcohol
GB1491529A (en) Oxidation catalyst
Tanaka et al. Reactive intermediates for the ethene homologation reaction on molybdena–silica catalysts
US4233248A (en) Process for oxidation of methanol to formaldehyde with nitrous oxide
Takita et al. Oxidation of ketones over metal oxide catalysts. II. Biacetyl synthesis over Co3O4-lanthanoid oxide catalysts.
Hardacre et al. Hydrogen bromide promoted oxidation in the gas phase
JPS557227A (en) Preparation of urethane
JPS61172851A (en) Method of dimerization of orthophthalic ester through oxidation and dehydrogenation
JPS565471A (en) Preparation of ethylene oxide
US1998218A (en) Catalyst and process for production of acetic acid
US3875240A (en) Synthesis of aldehydes
Hutchings et al. Effect of O3 versus O2 as Oxidants for Methane