GB1455645A - Production of aliphatic or cycloaliphatic dialdehydes and/or acetals of the same production of 3-sulphopropionic anhydride - Google Patents

Production of aliphatic or cycloaliphatic dialdehydes and/or acetals of the same production of 3-sulphopropionic anhydride

Info

Publication number
GB1455645A
GB1455645A GB1521574A GB1521574A GB1455645A GB 1455645 A GB1455645 A GB 1455645A GB 1521574 A GB1521574 A GB 1521574A GB 1521574 A GB1521574 A GB 1521574A GB 1455645 A GB1455645 A GB 1455645A
Authority
GB
United Kingdom
Prior art keywords
aliphatic
production
cycloaliphatic
acetals
same
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
GB1521574A
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.)
BASF SE
Original Assignee
BASF SE
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
Priority claimed from DE19732317625 external-priority patent/DE2317625C3/en
Application filed by BASF SE filed Critical BASF SE
Publication of GB1455645A publication Critical patent/GB1455645A/en
Expired legal-status Critical Current

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/20—Carbonyls
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1845—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing phosphorus
    • B01J31/185—Phosphites ((RO)3P), their isomeric phosphonates (R(RO)2P=O) and RO-substitution derivatives thereof
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/24—Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
    • B01J31/2404—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C43/00—Ethers; Compounds having groups, groups or groups
    • C07C43/30—Compounds having groups
    • C07C43/303—Compounds having groups having acetal carbon atoms bound to acyclic carbon atoms
    • 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
    • C07C45/49—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide
    • C07C45/50—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide by oxo-reactions
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82—Metals of the platinum group
    • B01J2531/822—Rhodium

Abstract

1455645 Aliphatic or cycloaliphatic dialdehydes and/or acetals of the same BASF AG 5 April 1974 [7 April 1973] 15215/74 Heading C2C The invention comprises a process for the production of an aliphatic or cycloaliphatic dialdehyde or an acetal of the same by reaction of an aliphatic or cycloaliphatic conjugated diene with carbon monoxide and hydrogen in the presence of a rhodium catalyst (which has been modified with a tertiary phosphine or phosphite) at a temperature of from 70‹ to 160‹ C. and at a pressure of from 100 to 600 atmospheres absolute, wherein the catalyst used is a rhodium complex which contains carbon monoxide, a tertiary organic phosphine or a tertiary organic phosphite and a halogen atom as ligands. It is advantageous to carry out the reaction in the presence of an alkanol or alkane diol as a solvent.
GB1521574A 1973-04-07 1974-04-05 Production of aliphatic or cycloaliphatic dialdehydes and/or acetals of the same production of 3-sulphopropionic anhydride Expired GB1455645A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19732317625 DE2317625C3 (en) 1973-04-07 Process for the preparation of aliphatic or cycloaliphatic dialdehydes and / or their acetals

Publications (1)

Publication Number Publication Date
GB1455645A true GB1455645A (en) 1976-11-17

Family

ID=5877389

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1521574A Expired GB1455645A (en) 1973-04-07 1974-04-05 Production of aliphatic or cycloaliphatic dialdehydes and/or acetals of the same production of 3-sulphopropionic anhydride

Country Status (7)

Country Link
JP (1) JPS5846491B2 (en)
BE (1) BE813363A (en)
CA (1) CA1023387A (en)
FR (1) FR2224428B1 (en)
GB (1) GB1455645A (en)
IT (1) IT1005691B (en)
NL (1) NL179273C (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0028378A1 (en) * 1979-10-26 1981-05-13 Union Carbide Corporation Improved hydroformylation process using stable rhodium catalyst
US4496769A (en) * 1982-06-11 1985-01-29 Davy Mckee (London) Limited Process for the preparation of aldehydes by hydroformylation of olefins
US4496768A (en) * 1982-06-11 1985-01-29 Davy Mckee Limited Process for the production of aldehydes by hydroformylation of alpha-olefins
US4507508A (en) * 1982-05-11 1985-03-26 Imperial Chemical Industries Plc Process for the production of unsaturated mono- or saturated dialdehydes and acetals thereof

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2849742B2 (en) * 1978-11-16 1980-10-16 Henkel Kgaa, 4000 Duesseldorf Process for the production of aldehydes and use of the process products as fragrances
DE2914090A1 (en) * 1979-04-07 1980-10-23 Henkel Kgaa USE OF ALDEHYDES AS ANTIMICROBIAL ACTIVE SUBSTANCES
US5312996A (en) * 1992-06-29 1994-05-17 Union Carbide Chemicals & Plastics Technology Corporation Hydroformylation process for producing 1,6-hexanedials
KR102098429B1 (en) * 2012-12-06 2020-04-07 다우 테크놀로지 인베스트먼츠 엘엘씨. Hydroformylation process

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0028378A1 (en) * 1979-10-26 1981-05-13 Union Carbide Corporation Improved hydroformylation process using stable rhodium catalyst
US4507508A (en) * 1982-05-11 1985-03-26 Imperial Chemical Industries Plc Process for the production of unsaturated mono- or saturated dialdehydes and acetals thereof
US4496769A (en) * 1982-06-11 1985-01-29 Davy Mckee (London) Limited Process for the preparation of aldehydes by hydroformylation of olefins
US4496768A (en) * 1982-06-11 1985-01-29 Davy Mckee Limited Process for the production of aldehydes by hydroformylation of alpha-olefins

Also Published As

Publication number Publication date
FR2224428A1 (en) 1974-10-31
NL179273B (en) 1986-03-17
NL179273C (en) 1986-08-18
JPS5046614A (en) 1975-04-25
NL7404631A (en) 1974-10-09
JPS5846491B2 (en) 1983-10-17
BE813363A (en) 1974-10-07
DE2317625B2 (en) 1975-12-11
IT1005691B (en) 1976-09-30
FR2224428B1 (en) 1978-07-28
DE2317625A1 (en) 1974-10-24
CA1023387A (en) 1977-12-27

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee