GB929648A - Improvements in and relating to improving the quality of alcohols - Google Patents

Improvements in and relating to improving the quality of alcohols

Info

Publication number
GB929648A
GB929648A GB91160A GB91160A GB929648A GB 929648 A GB929648 A GB 929648A GB 91160 A GB91160 A GB 91160A GB 91160 A GB91160 A GB 91160A GB 929648 A GB929648 A GB 929648A
Authority
GB
United Kingdom
Prior art keywords
alcohol
sulphuric acid
quality
improving
distilled
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
GB91160A
Inventor
Ronald Walter Fawcett
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries 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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB91160A priority Critical patent/GB929648A/en
Priority to DEJ19260A priority patent/DE1168879B/en
Priority to SE18661A priority patent/SE315874B/xx
Priority to CH32161A priority patent/CH411818A/en
Publication of GB929648A publication Critical patent/GB929648A/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
    • C07C29/74Separation; Purification; Use of additives, e.g. for stabilisation
    • C07C29/88Separation; Purification; Use of additives, e.g. for stabilisation by treatment giving rise to a chemical modification of at least one compound
    • 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
    • C07C29/74Separation; Purification; Use of additives, e.g. for stabilisation
    • C07C29/76Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment
    • C07C29/86Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment by liquid-liquid treatment

Landscapes

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

Abstract

The quality of an oxo alcohol is improved by mixing it with sulphuric acid and separating the alcohol from the resulting mixture. The process is particularly suitable for improving the quality of oxo alcohols containing 7 or more carbon atoms. The process may be applied to crude oxo alcohols but preferably the crude product is previously refined to give an alcohol product boiling over a narrow range of temperature. Generally the amount of sulphuric acid used is 0.001-0.1% by weight of the alcohol although amounts up to 0.8% may be used. The sulphuric acid may be used in concentrated form and the mixture then distilled. Alternatively, the alcohol may be mixed with water and sulphuric acid, the alcohol layer then being separated from the aqueous layer, washed with water and distilled. The aqueous solution of sulphuric acid preferably contains up to 25% by weight of acid. The alcohol is contacted with the sulphuric acid at room temperature or above, e.g. up to 80 DEG C. Reference has been directed by the Comptroller to Specification 874,583.
GB91160A 1960-01-11 1960-01-11 Improvements in and relating to improving the quality of alcohols Expired GB929648A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
GB91160A GB929648A (en) 1960-01-11 1960-01-11 Improvements in and relating to improving the quality of alcohols
DEJ19260A DE1168879B (en) 1960-01-11 1961-01-04 Process for the purification of alcohols of the oxo synthesis
SE18661A SE315874B (en) 1960-01-11 1961-01-10
CH32161A CH411818A (en) 1960-01-11 1961-01-11 Process for improving the quality of alcohols, produced using the oxo process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB91160A GB929648A (en) 1960-01-11 1960-01-11 Improvements in and relating to improving the quality of alcohols

Publications (1)

Publication Number Publication Date
GB929648A true GB929648A (en) 1963-06-26

Family

ID=9712673

Family Applications (1)

Application Number Title Priority Date Filing Date
GB91160A Expired GB929648A (en) 1960-01-11 1960-01-11 Improvements in and relating to improving the quality of alcohols

Country Status (4)

Country Link
CH (1) CH411818A (en)
DE (1) DE1168879B (en)
GB (1) GB929648A (en)
SE (1) SE315874B (en)

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE814739C (en) * 1949-08-06 1951-09-24 Ruhrchemie Ag Process for purifying synthetic aldehyde products
DE910539C (en) * 1951-04-28 1954-05-03 Ruhrchemie Ag Process for the preparation of acetal-free fractions from the products of caroxydrogenation
DE953606C (en) * 1954-04-03 1956-12-06 Chemische Verwertungsgesellsch Process for purifying oxygen-containing organic compounds

Also Published As

Publication number Publication date
DE1168879B (en) 1964-04-30
SE315874B (en) 1969-10-13
CH411818A (en) 1966-04-30

Similar Documents

Publication Publication Date Title
GB1037693A (en) Hydrogenation of salts of phthalic acids
Burton et al. 417. Acylation reactions catalysed by strong acids. Part II.“Acetyl perchlorate” as a C-acetylating agent
US2010356A (en) Mixed tertiary ethers
GB1017605A (en) Improvements in or relating to the preparation of dialkyl terephthalates
GB929648A (en) Improvements in and relating to improving the quality of alcohols
GB965048A (en) Tetrafluoro-dichloroisopropanol and its hydrate and the production thereof
GB298137A (en) Improved process for concentrating acetic acid
GB722390A (en) Separating methyl acetate from other organic compounds by extractive distillation
GB956115A (en) Improvements in or relating to a process for the preparation of organic peroxides
US2243701A (en) Process for producing butanol-(1)-one-(3)
US2974170A (en) Preparation of nuclearly unsaturated ionones and intermediates therefor
GB936373A (en) Improvements in or relating to the production of esters of boron-containing acids
GB769813A (en) Improvements in the production of cyclopentadiene by deploymerisation of dicyclopentadiene
GB822535A (en) Improvements in or relating to a process for separately recovering an aldehyde or ketone and an aqueous solution of the corresponding alcohol from an aqueous mixture containing the aldehyde or ketone and the alcohol
GB866182A (en) Process for the preparation of unsaturated nitriles
GB580102A (en) Improvements in or relating to the fractional distillation of hydrocarbons
GB755528A (en) Improved dehydrogenation process
Burton XXXVI.—Mobile anion tautomerism. Part IV. The stability of some α-and γ-alkylallyl alcohols and their esters. 2: 4-Dimethylcinnamyl alcohol
GB776056A (en) Process for the production of unsaturated ethers
GB601901A (en) Improvements in or relating to the manufacture of ethylcaproic acid, esters thereof and compositions containing said esters
GB1023856A (en) Method for purifying aqueous solutions of methylbutynol
GB813018A (en) A method for the preparation of isomeric tertiary alcohols
GB791747A (en) Alcohol hydrofinishing
GB843751A (en) A process for the preparation of unsaturated ionones
GB654494A (en) Process for the preparation of ditolylethane