GB811131A - Improvements in or relating to method of preparing new carboxylic acid and the new carboxylic acid resulting from said method - Google Patents

Improvements in or relating to method of preparing new carboxylic acid and the new carboxylic acid resulting from said method

Info

Publication number
GB811131A
GB811131A GB27377/56A GB2737756A GB811131A GB 811131 A GB811131 A GB 811131A GB 27377/56 A GB27377/56 A GB 27377/56A GB 2737756 A GB2737756 A GB 2737756A GB 811131 A GB811131 A GB 811131A
Authority
GB
United Kingdom
Prior art keywords
bis
aliphatic
ether
hydroxy
chloroethyl
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
GB27377/56A
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.)
SC Johnson and Son Inc
Original Assignee
SC Johnson and Son Inc
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 SC Johnson and Son Inc filed Critical SC Johnson and Son Inc
Publication of GB811131A publication Critical patent/GB811131A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/40Unsaturated compounds
    • C07C59/58Unsaturated compounds containing ether groups, groups, groups, or groups
    • C07C59/64Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Epoxy Resins (AREA)
  • Lubricants (AREA)

Abstract

A polycarboxylic acid is made by condensing an aliphatic coupling agent and a bis-(hydroxy-aryl)-substituted aliphatic acid, said aliphatic coupling agent being an epihalohydrin, an aliphatic dihalide, an aliphatic dihaloether or an aliphatic polyepoxide. Specified coupling agents are 1,2 - dichloroethane, 1,3 - dichloro-propane, 1,4 - dichlorobutane, 1,4 - dichloro-butene, glycol dichlorohydrin, bis-(2-chloro-ethyl) ether, epichlorohydrin, epibromohydrin, 2,3 - epoxypropyl - 2 - hydroxy - 3 - chloropropyl ether, 1,2 - epoxy - 3,4 - epoxybutane and bis-(2,3-epoxypropyl) ether. In the examples, 4,4 - bis - (4 - hydroxy - phenyl) - pentanoic acid is condensed in aqueous caustic soda with: (I) 1,4 - dichlorobutene - 2; (II) 1,4 - dichloro-butane; (III) and (IV) bis-(2-chloroethyl)ether; (V) and (VI) bis-(4-hydroxy-phenyl)-isopropylidene and bis-(2-chloroethyl) ether and (VII) to (X) inclusive epichlorohydrin. The resultant resinous polycarboxylic acids may be esterified with alcoholic hydroxyl groups or epoxide groups and may be used as coatings. The acids may be condensed with polyhydric phenol/epichlorohydrin reaction products and epoxidised vegetable oils. Example (XI) describes the reaction of the product of Example (I) with an epoxidised soya bean oil to form a film. Specifications 768,206 and 790,373 are referred to.ALSO:A polycarboxylic acid is made by condensing an aliphatic coupling agent and a bis (hydroxy aryl) substituted aliphatic acid, said aliphatic coupling agent being an epihalohydrin, an aliphatic dihalide, an aliphatic dihaloether, or an aliphatic poly epoxide. Specified coupling agents are 1,2-dichloro ethane, 1,3-dichloropropane, 1,4 - dichlorobutane, 1,4 - dichlorobutene, glycol dichlorohydrin, bis - (2 - chloroethyl) ether, epichlorohydrin, epibromohydrin, 2,3 - epoxy propyl 2 - hydroxy - 3 - chloropropyl ether, 1,2 - epoxy - 3,4 - epoxybutane, and bis - (2,3 - epoxypropyl) ether. In the examples, 4,4-bis-(4-hydroxy-phenyl) pentanoic acid is condensed in aqueous caustic soda with: (I) 1,4-dichlorobutene-2, (II) 1,4-dichlorobutane, (III) and (IV) bis-(2-chloroethyl) ether, (V) and (VI) bis-(4-hydroxy phenyl) isopropylidene and bis-(2-chloroethyl) ether and (VII) to (X) inclusive epichlorohydrin. Specifications 768,206 and 790,373 are referred to.
GB27377/56A 1955-10-03 1956-09-06 Improvements in or relating to method of preparing new carboxylic acid and the new carboxylic acid resulting from said method Expired GB811131A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US811131XA 1955-10-03 1955-10-03

Publications (1)

Publication Number Publication Date
GB811131A true GB811131A (en) 1959-04-02

Family

ID=22162171

Family Applications (1)

Application Number Title Priority Date Filing Date
GB27377/56A Expired GB811131A (en) 1955-10-03 1956-09-06 Improvements in or relating to method of preparing new carboxylic acid and the new carboxylic acid resulting from said method

Country Status (1)

Country Link
GB (1) GB811131A (en)

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