GB303917A - Improvements in the production of sulphonic acids - Google Patents

Improvements in the production of sulphonic acids

Info

Publication number
GB303917A
GB303917A GB23964/27A GB2396427A GB303917A GB 303917 A GB303917 A GB 303917A GB 23964/27 A GB23964/27 A GB 23964/27A GB 2396427 A GB2396427 A GB 2396427A GB 303917 A GB303917 A GB 303917A
Authority
GB
United Kingdom
Prior art keywords
acid
treated
propylene
anhydride
mixture
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
GB23964/27A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to GB23964/27A priority Critical patent/GB303917A/en
Publication of GB303917A publication Critical patent/GB303917A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C303/00Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
    • C07C303/02Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof
    • C07C303/04Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof by substitution of hydrogen atoms by sulfo or halosulfonyl groups
    • C07C303/06Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof by substitution of hydrogen atoms by sulfo or halosulfonyl groups by reaction with sulfuric acid or sulfur trioxide
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/12Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/16Systems containing only non-condensed rings with a six-membered ring the ring being unsaturated

Landscapes

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

Abstract

303,917. Johnson, J. Y., (I. G Farbenindustrie Akt.-Ges.). Sept 12, 1927. Samples furnished. Emulsions, making.-Sulphonic acids useful as emulsifying agents are obtained from unsaturated aliphatic hydrocarbons or their halogen derivatives or from unsaturated hydroaromatic compounds by treating them with sulphonating agents, such as sulphuric acid, sulphur trioxide, and/or chlorsulphonic acid, and an equimolecular amount or more of an organic acid, acid anhydride, or acid chloride or of phosphoric acid ur its anhydride or chloride. The reaction may be applied to the individual hydrocarbons or compounds or to mixtures containing a preponderating proportion thereof such as petroleum or its cracking products or brown-coal tar oils such as gas oil, yellow oil, and solar oil; such mixtures may be treated directly or after enriching or isolating their olefine constituents. In one example, tetrahydrobenzene is treated with a mixture of sulphuric acid and acetic anhydride and the reaction product is diluted with water, heated to remove acetic acid, and neutralized. Derivatives of unsaturated hydroaromatic hydrocarbons, such as the corresponding napbthenic acids, may be treated in the same way. In another example, propylene is led into a mixture of sulphuric acid and acetic anhydride and the mixture is allowed to stand. The reaction product so obtained is worked up by diluting with water, boiling under reflux, and distilling off acetic acid. The sulphonated propylene can be recovered from the solution as calcium or sodium salt. Higher homologues or propylene or halogen derivatives of the olefines such as trichlorethylene. may be treated in the same way.
GB23964/27A 1927-09-12 1927-09-12 Improvements in the production of sulphonic acids Expired GB303917A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB23964/27A GB303917A (en) 1927-09-12 1927-09-12 Improvements in the production of sulphonic acids

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB23964/27A GB303917A (en) 1927-09-12 1927-09-12 Improvements in the production of sulphonic acids

Publications (1)

Publication Number Publication Date
GB303917A true GB303917A (en) 1929-01-14

Family

ID=10204210

Family Applications (1)

Application Number Title Priority Date Filing Date
GB23964/27A Expired GB303917A (en) 1927-09-12 1927-09-12 Improvements in the production of sulphonic acids

Country Status (1)

Country Link
GB (1) GB303917A (en)

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