GB663240A - Synthesis of octyl alcohols - Google Patents

Synthesis of octyl alcohols

Info

Publication number
GB663240A
GB663240A GB8360/49A GB836049A GB663240A GB 663240 A GB663240 A GB 663240A GB 8360/49 A GB8360/49 A GB 8360/49A GB 836049 A GB836049 A GB 836049A GB 663240 A GB663240 A GB 663240A
Authority
GB
United Kingdom
Prior art keywords
olefine
cobalt
reaction zone
feed
liquid
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
GB8360/49A
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.)
Standard Oil Development Co
Original Assignee
Standard Oil Development 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 Standard Oil Development Co filed Critical Standard Oil Development Co
Publication of GB663240A publication Critical patent/GB663240A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C27/00Processes involving the simultaneous production of more than one class of oxygen-containing compounds
    • C07C27/20Processes involving the simultaneous production of more than one class of oxygen-containing compounds by oxo-reaction
    • C07C27/22Processes involving the simultaneous production of more than one class of oxygen-containing compounds by oxo-reaction with the use of catalysts which are specific for this process
    • 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

Abstract

Oxygenated compounds are made by reacting heptenes with carbon monoxide and hydrogen at 300-360 DEG C. and 2900-3500 p.s.i. in the presence of a cobalt salt of a fatty acid so that a body of cobalt material is maintained in the reaction zone and the quantity of cobalt compound calculated as metal dissolved in and removed from the reaction zone in the effluent is of the same order as the cobalt compound calculated as metal added with the feed. Products from the carbonylation zone are preferably cooled and separated into liquid and gaseous phases and the gaseous phase and at least part of the liquid phase recycled to the reaction zone, c.f. Specification 647,363. The remainder of the liquid phase is treated in the normal fashion for alcohol production. In an illustration a C7 olefine non-selective polymer cut is mixed with cobalt naphthenate, the weight of Co in solution being 0.1-0.3, preferably 0.15-0.3 per cent, of total liquid, preheated to 475-525 DEG F., and passed to the bottom of a primary reactor which may contain conventional packing. Hydrogen and carbon monoxide is approximate vol. ratio of 1.0 to 1.2 : 1 is fed to the reactor and may be fresh feed or recycled gas and synthesis is effected at 2900-3500 p.s.i., preferably at about 3000 p.s.i., and at 300-360 DEG F., preferably 340-360 DEG F., with an olefine fresh feed rate of from about 0.4-0.6, a fresh synthesis gas feed rate of 2000-3000 cu. feet/barrel of olefine and a nominal residence time of olefine of about 2 1/2 hours. Cooling of the reactor is effected by recycling product, as described above in the preferred treatment of the product. Recycle gas rate is about 6000 cu. feet/barrel of olefine feed. The product before decobalting may be purged with hydrogen, c.f. Specification 629,915, and hydrogenation is preferably effected at about 400-500 DEG F., about 2800-3200 p.s.i., with a liquid feed rate of about 0.6 v./v./hour and a recycle gas rate of about 15,000 cu. feet/barrel. A number of conventional hydrogenation catalysts are specified. The hydrogenated product is purified and an octanol cut of boiling range 350-375 DEG F. taken. Tables are provided which show the effect of temperature variation in which higher or lower temperatures than those specified result respectively in accumulating or stripping the cobalt in the reaction zone, and of other reaction variables in two runs to produce octanols.
GB8360/49A 1948-08-12 1949-03-28 Synthesis of octyl alcohols Expired GB663240A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US663240XA 1948-08-12 1948-08-12

Publications (1)

Publication Number Publication Date
GB663240A true GB663240A (en) 1951-12-19

Family

ID=22068774

Family Applications (1)

Application Number Title Priority Date Filing Date
GB8360/49A Expired GB663240A (en) 1948-08-12 1949-03-28 Synthesis of octyl alcohols

Country Status (1)

Country Link
GB (1) GB663240A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE960186C (en) * 1952-03-01 1957-03-21 Chemische Verwertungsgesellsch Process for the preparation of oxygen-containing compounds
DE1115727B (en) * 1959-01-23 1961-10-26 Hoechst Ag Process for the production of aldehydes by the oxo synthesis
US4518809A (en) * 1981-06-11 1985-05-21 Monsanto Company Preparation of pentyl nonanols

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE960186C (en) * 1952-03-01 1957-03-21 Chemische Verwertungsgesellsch Process for the preparation of oxygen-containing compounds
DE1115727B (en) * 1959-01-23 1961-10-26 Hoechst Ag Process for the production of aldehydes by the oxo synthesis
US4518809A (en) * 1981-06-11 1985-05-21 Monsanto Company Preparation of pentyl nonanols

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