GB947550A - Method of rendering alcohols anhydrous - Google Patents

Method of rendering alcohols anhydrous

Info

Publication number
GB947550A
GB947550A GB1406262A GB1406262A GB947550A GB 947550 A GB947550 A GB 947550A GB 1406262 A GB1406262 A GB 1406262A GB 1406262 A GB1406262 A GB 1406262A GB 947550 A GB947550 A GB 947550A
Authority
GB
United Kingdom
Prior art keywords
anhydrous
molecular proportion
alcohols
butyl
amyl
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
GB1406262A
Inventor
David Duerden
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.)
Abbott Laboratories
Original Assignee
Abbott Laboratories
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 Abbott Laboratories filed Critical Abbott Laboratories
Priority to GB1406262A priority Critical patent/GB947550A/en
Publication of GB947550A publication Critical patent/GB947550A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D3/00Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
    • B01D3/001Processes specially adapted for distillation or rectification of fermented solutions

Abstract

Alcohols containing 1-5 carbons are made anhydrous by (a) dissolving sodium or potassium in a water-alkanol mixture, at least two atomic proportions of sodium or potassium being used for each molecular proportion of water present; (b) passing sulphur dioxide, sodium metabisulphite or potassium bisulphite into the resulting solution, at least one molecular proportion of sulphur dioxide or half a molecular proportion of metabisulphite being used for each molecular proportion of water present in the mixture; and (c) continuing the reaction at boiling temperature under reflux until the precipitation of the alkali metal sulphite is complete and the alkanol is substantially anhydrous. Examples describe the preparation of anhydrous methyl, ethyl, isoamyl and isopropyl alcohols. The process is stated to be suitable for the preparation of anhydrous n-propyl, n-butyl, isobutyl, sec-butyl, tert.-butyl, n-amyl, sec-amyl, and tert.-amyl alcohols.
GB1406262A 1962-04-11 1962-04-11 Method of rendering alcohols anhydrous Expired GB947550A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1406262A GB947550A (en) 1962-04-11 1962-04-11 Method of rendering alcohols anhydrous

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1406262A GB947550A (en) 1962-04-11 1962-04-11 Method of rendering alcohols anhydrous

Publications (1)

Publication Number Publication Date
GB947550A true GB947550A (en) 1964-01-22

Family

ID=10034308

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1406262A Expired GB947550A (en) 1962-04-11 1962-04-11 Method of rendering alcohols anhydrous

Country Status (1)

Country Link
GB (1) GB947550A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0070441A1 (en) * 1981-07-20 1983-01-26 Improtec Extractive distillation process for the production of fuel grade alcohols

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0070441A1 (en) * 1981-07-20 1983-01-26 Improtec Extractive distillation process for the production of fuel grade alcohols

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