GB539281A - Improvements in or relating to the preparation of aliphatic substituted aromatic sulphonic acids and salts thereof - Google Patents

Improvements in or relating to the preparation of aliphatic substituted aromatic sulphonic acids and salts thereof

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Publication number
GB539281A
GB539281A GB3964/40A GB396440A GB539281A GB 539281 A GB539281 A GB 539281A GB 3964/40 A GB3964/40 A GB 3964/40A GB 396440 A GB396440 A GB 396440A GB 539281 A GB539281 A GB 539281A
Authority
GB
United Kingdom
Prior art keywords
acid
aliphatic
alcohol
sulphur dioxide
compositions
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
GB3964/40A
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.)
Colgate Palmolive Co
Original Assignee
Colgate Palmolive 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 Colgate Palmolive Co filed Critical Colgate Palmolive Co
Publication of GB539281A publication Critical patent/GB539281A/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/01Sulfonic acids
    • C07C309/28Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • 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

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

Abstract

539,281. Alkylated and acylated aromatic sulphonic acids; wetting &c. agents. COLGATE-PALMOLIVE-PEET CO. March 2, 1940, No. 3964. Convention date, March 4, 1939. [Classes 2 (iii) and 15 (ii)] [Also in Group III] Aliphatic substituted aromatic compounds in which the aliphatic radicle contains at least 6 carbon atoms are sulphonated in a solvent comprising liquid sulphur dioxide as the major constituent. The formation of the aliphatic substituted aromatic compound may be effected before the sulphonation as a separate step or simultaneously therewith. Aliphatic compounds for the nuclear substitution are olefines, carboxylic acid halides, aliphatic halogenated compounds and aliphatic alcohols. The following aliphatic compounds are specified: hexene to undecene, tetradecene, hexadecene, octadecene, cerotene, cyclohexene, cracked and dehydrogenated petroleums, polymerised isobutylene, polymerised isoamylene, benzoylchloride, stearoylchloride, lauroylchloride, myristoyl chloride, hexyl to dodecylalcohol, myristyl, cetyl, octadecyl, oleyl, montanyl and carnaubyl alcohol, octa-decandiol, ceryl, cyclohexyl, methylcyclohexyl, and melissyl alcohols, alcohols derived from cocobutter, soya bean, tallow, cottonseed, talloil, Japan wax, China wax, montan wax, ceresine, ozocerite, stearone and laurone and olefines derived from these alcohols by dehydration. By processes of catalytic dehydrogenation, halogenation, cracking and dehydrohalogenation aliphatic compounds suitable for the nuclear substitution may be prepared from any liquid or solid paraffin such as mineral oils, petroleum jelly, liquid petrolatum, hydrocarbons obtained by distilling, cracking, reducing or hydrogenating mineral oils, tars, oxides of carbon and schist oils, lignite wax, brown coal and ceresin. The halogenation of the hydrocarbons may be effected in the presence of the aromatic component. The aromatic compounds may contain more,than one aliphatic substituent and the aliphatic compounds may be linked with more than one aromatic radicle. Suitable aliphatic compounds for the latter process are octadecenylchloride, octadecadiene, octadecenyl alcohol, octadecandiol, dichloroctadecane, dichlordodecane. Halogenated fatty acids, hydroxy fatty acids, mono and poly olefinic fatty acids, monochlorpalmitic acid, linoleic acid, dichlorstearic acid, ricinoleic acid, lauroyl glycerolmonochlorhydrin, tetraethylene glycol, ethyloleate, octadecenylethylether, dodecylchloracetate and dichlorlaurone are also mentioned. Specified aromatic compounds which may be used are, toluene, xylene, cumene, cymeme, ethylbenzene, acenaphthene, phenanthrene, anthracene, methylnaphthalene, ethylnaphthalene, tetrahydronaphthalene, triphenylmethane, diphenylmethane, fluorene, styrene, indene; coumarone, coal tar fractions or extracts, benzylchloride, phenanthrone, acetophenone, diphenylketone, diphenyloxide, veratrol, benzylalcohol, phenols, alkylolphenols, hydroquinone, resorcinol and halogen derivatives. Furfural, kojic acid and cyclopentadienes are mentioned. The alkylation or acylation may be assisted by solvents such as benzene, methane, butane, ethylene, petroleum ether, dioxane, ether, carbonbisulphide, carbontetrachloride, chloroform, dichlorethane, trichlorethylene and dichlordifluormethane as well as liquid sulphur dioxide, and refrigeration may be effected by partial evaporation. For the sulphonation, sulphuric acid, oleum, sulphonylchloride, a mixture of sulphurdioxide and chlorine, sulphur trioxide, acetylsulphuric acid, bromsulphonic acid and chlorsulphonic acid may be used and assistants such as acetic anhydride and chloride, glacial acetic acid, propionic, boric and butyric anhydride and phosphorus pentoxide. The product which may contain more than one sulphonic group may be worked up by adding water to cause the formation of layers or by extracting the solid salts formed by neutralization by means of solvents such as alcohol, dioxane, acetone or butyl alcohol. In the neutralization, alkalies, ammonia, mono-, di-, or tri-, ethanolamine, mono-, di- or triglycerolamine, pyridine or piperidine may be used. Calcium, lithium, magnesium and mercury salts are'also mentioned. Aluminium-chloride, boronfluoride, bromides and chlorides of iron, zinc, antimony, boron, tin, titanium and indium, floridin, tonsil, fullers earth and sulphuric acid and its acid derivatives may be used as catalysts for the alkylation process. The products, which are stated to have wetting, solubilizing, detergent, water softening, dispersing, penetrating and equalizing properties may be used in association with soap, rosinates, long chain alcohol sulphates, monoglyceridesulphates, sulphonated mineral oil extracts, turkey red oil, lecithin, glycerolamines, di- and triethanolamines, sodium carbonate, silicate and phosphate, borax, dyes, lakes, pigments, abrasives, silica, pumice, feldspar, chalk, infusorial earth, bentonite, talc, starch, carbontetrachloride, perchlorethylene, glycerol, alcohol, glycoltetrahydrofurfuryl alcohol, phenol, cyclohexa n o 1, tetrahydronaphthalene, pin e oil, mineral oils, deodorants, fats, oils, fatty acids, monoglycerides, vitamins, waxes, gums, glue, resins, phenylmercurychloride, hydroxybenzoicmethylester, mercurychloride, aluminium chloride, sodium sulphate, chloride, acetate, bicarbonate, hypochlorite, thiosulphate, hydrosulphite and hyposulphate and similar potassium and ammonium salts, tetraphosphoric acid, hexametaphosphoric acid, pyrophosphoric acid and their alkali metal, ammonia and amine salts or alkyl esters. The compositions may be used as or in insecticides, cements, antiseptics, water softeners, disinfectants, water paints, polishes, sizes, glues, shellac and casein compositions, tooth and mouth detergents, laundry blueing, bleaching, dyeing, softening, lubricating and discharging compositions, depilatories, dust preventing compositions, antifreezing, anti-fogging and anti-corrosion compositions, wood impregnants, electrolytic baths, etching compositions, cosmetics, shaving preparations, shampoos, hair lotions, tanning agents, fat liquors, photographic solutions, paint, varnish and grease removers, dry cleaners, petroleum de-emulsifying compositions, lypolitics preparations of resins and plasticizers such as aliphatic substituted phenolaldehyde, aliphatic substituted arylsulphonamide and aliphatic substituted arylsulphonamidealdehyde resins. In examples: (1) dodecylchloride is condensed with benzene in the presence of liquid sulphur dioxide and aluminiumchloride in an autoclave and the product sulphonated by means of a mixture of oleum and liquid sulphur dioxide, it is finally added to ice water, neutralized, extracted with gasoline and dried: (2) naphthalene is condensed with diisoamylene and sulphonated and the product washed with ether, neutralized and extracted with isopropyl alcohol: (3) diphenyl dissolved in dichorethane is treated with a liquid sulphur dioxide extract of cracked mineral oil, 96 per cent sulphuric acid being used for the condensation; the product is sulphonated in liquid sulphur dioxide, ice water added and the resulting three layers separated; the middle layer, after washing with liquid sulphur dioxide is freed from dissolved sulphur dioxide, washed with an aqueous solution of sodium chloride and sulphate, neutralised with soda and sprayed into hot gases. The process may be conducted in a continuous manner.
GB3964/40A 1939-03-04 1940-03-02 Improvements in or relating to the preparation of aliphatic substituted aromatic sulphonic acids and salts thereof Expired GB539281A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US539281XA 1939-03-04 1939-03-04

Publications (1)

Publication Number Publication Date
GB539281A true GB539281A (en) 1941-09-03

Family

ID=21987508

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3964/40A Expired GB539281A (en) 1939-03-04 1940-03-02 Improvements in or relating to the preparation of aliphatic substituted aromatic sulphonic acids and salts thereof

Country Status (1)

Country Link
GB (1) GB539281A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2572605A (en) * 1948-04-01 1951-10-23 Monsanto Chemicals Process for sulfonation of organic compounds
US2616936A (en) * 1949-04-12 1952-11-04 Universal Oil Prod Co Method of sulfonation with sulfur trioxide
US2723990A (en) * 1949-12-24 1955-11-15 Allied Chem & Dye Corp Process for sulfonating detergent alkylates
US3238249A (en) * 1960-09-23 1966-03-01 Exxon Research Engineering Co Alkylbenzene sulfonate production via n-olefin dimerization
US3240280A (en) * 1962-12-26 1966-03-15 Phillips Petroleum Co Drilling and/or servicing of wells

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2572605A (en) * 1948-04-01 1951-10-23 Monsanto Chemicals Process for sulfonation of organic compounds
US2616936A (en) * 1949-04-12 1952-11-04 Universal Oil Prod Co Method of sulfonation with sulfur trioxide
US2723990A (en) * 1949-12-24 1955-11-15 Allied Chem & Dye Corp Process for sulfonating detergent alkylates
US3238249A (en) * 1960-09-23 1966-03-01 Exxon Research Engineering Co Alkylbenzene sulfonate production via n-olefin dimerization
US3240280A (en) * 1962-12-26 1966-03-15 Phillips Petroleum Co Drilling and/or servicing of wells

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