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GB1041101A - Oxo process - Google Patents

Oxo process

Info

Publication number
GB1041101A
GB1041101A GB2664A GB2664A GB1041101A GB 1041101 A GB1041101 A GB 1041101A GB 2664 A GB2664 A GB 2664A GB 2664 A GB2664 A GB 2664A GB 1041101 A GB1041101 A GB 1041101A
Authority
GB
United Kingdom
Prior art keywords
temperature
oxonation
propylene
reactor
hydrogen
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
GB2664A
Inventor
Arthur Heinsch William Robert
John William Anderson
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.)
Monsanto Co
Original Assignee
Monsanto Co
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 Monsanto Co filed Critical Monsanto Co
Priority to GB2664A priority Critical patent/GB1041101A/en
Publication of GB1041101A publication Critical patent/GB1041101A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/16Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxo-reaction combined with reduction

Landscapes

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

Abstract

In a process for the preparation of alcohols by the oxo process wherein olefins are reacted with carbon monoxide and hydrogen in the presence of a cobalt catalyst at superatmospheric pressures, the improvement comprises controlling the temperature of the reaction mixture to provide a continuously increasing temperature, the initial temperature being 50-178 DEG C., the mid-point temperature 180-200 DEG C. and the terminal temperature 205-225 DEG C. The oxonation is effected in the presence of known cobalt sources, e.g. cobalt carbonyl, carboxylate, oxide, carbonate or metal, yielding in the reaction mixture cobalt carbonyl which is effective as both the carbonylation and hydrogenation catalyst. The preferred amount of hydrogen in the feed and product gas is less than 60% volume and 3-50% volume, respectively, based on total CO + H2 volume. In a preferred embodiment using a tubular reactor, the percentage of hydrogen in the gas phase decreases along the reactor and the numerical product of the value of this H2 percentage multiplied by the temperature at a particular point lies in the range 1500-10,000. It is preferred to introduce 2-10% by weight, based on total reaction mass, of water into the reactor. The process can be carried out, continuously or batchwise, in a tubular reactor, a series of autoclaves or a combination of tubular reactors and stirred autoclaves. Examples describe the oxonation of (1) propylene trimer to isodecyl alcohol, (7) propylene to n- and i-butyl alcohols, (8) heptene to isodecyl alcohol, (9), (10), (11) and (12), propylene tetramer to tridecyl alcohol. In Examples (2)-(6) temperatures outside the scope of the invention are used in the oxonation of propylene trimer to give reaction products containing considerable proportions of isodecylaldehyde.
GB2664A 1964-01-01 1964-01-01 Oxo process Expired GB1041101A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2664A GB1041101A (en) 1964-01-01 1964-01-01 Oxo process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2664A GB1041101A (en) 1964-01-01 1964-01-01 Oxo process

Publications (1)

Publication Number Publication Date
GB1041101A true GB1041101A (en) 1966-09-01

Family

ID=9697055

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2664A Expired GB1041101A (en) 1964-01-01 1964-01-01 Oxo process

Country Status (1)

Country Link
GB (1) GB1041101A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010527969A (en) * 2007-05-23 2010-08-19 シエル・インターナシヨナル・リサーチ・マートスハツペイ・ベー・ヴエー Hydroformylation process
JP2010527968A (en) * 2007-05-23 2010-08-19 シエル・インターナシヨナル・リサーチ・マートスハツペイ・ベー・ヴエー Hydroformylation process
US7781620B2 (en) 2006-12-21 2010-08-24 Shell Oil Company Hydroformylation process

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7781620B2 (en) 2006-12-21 2010-08-24 Shell Oil Company Hydroformylation process
JP2010527969A (en) * 2007-05-23 2010-08-19 シエル・インターナシヨナル・リサーチ・マートスハツペイ・ベー・ヴエー Hydroformylation process
JP2010527968A (en) * 2007-05-23 2010-08-19 シエル・インターナシヨナル・リサーチ・マートスハツペイ・ベー・ヴエー Hydroformylation process
US8017810B2 (en) 2007-05-23 2011-09-13 Shell Oil Company Hydroformulation process
US8017811B2 (en) 2007-05-23 2011-09-13 Shell Oil Company Hydroformylation process

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