GB551305A - Improvements in and relating to the preparation of hydroxy dithionaphthoic acids and their derivatives - Google Patents

Improvements in and relating to the preparation of hydroxy dithionaphthoic acids and their derivatives

Info

Publication number
GB551305A
GB551305A GB17080/40A GB1708040A GB551305A GB 551305 A GB551305 A GB 551305A GB 17080/40 A GB17080/40 A GB 17080/40A GB 1708040 A GB1708040 A GB 1708040A GB 551305 A GB551305 A GB 551305A
Authority
GB
United Kingdom
Prior art keywords
alkali metal
reaction
salts
hydroxy
converted
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
GB17080/40A
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.)
Wingfoot Corp
Original Assignee
Wingfoot Corp
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 Wingfoot Corp filed Critical Wingfoot Corp
Publication of GB551305A publication Critical patent/GB551305A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C327/00Thiocarboxylic acids

Landscapes

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

Abstract

551,305. Hydroxy dithio-naphthoic acids. WINGFOOT CORPORATION. Nov. 29, 1940, No. 17080. Convention date, Nov. 29, 1939. [Class 2 (iii)] [Also in Group V] Hydroxy dithio-naphthoic acid alkali salts are prepared by reacting in a common solvent a naphthol, an alkali metal hydroxide and carbon disulphide. It is preferred that the reaction be carried out under substantially anhydrous conditions, and the water formed in the reaction be removed as it is formed. An alternative procedure comprises the separate preparation of the alkali metal naphtholate which is then reacted with carbon disulphide. Solvents mentioned include ketones, pyridine, mixtures 'of aromatic or aliphatic hydrocarbons with acetone or other ketones, and mixtures of ethers and ketones. Numerous examples are given using as starting materials both α-, and #-naphthol. Varying reaction conditions are exemplified. If alkali metal is used instead of an alkali metal hydroxide, the formation of water in the reaction is avoided. The alkali metal salts prepared as above described may be converted into the free acid by treatment with a dilute mineral acid, or they may be converted into basic zinc salts by treatment with an aqueous solution of zinc sulphate, or they may be converted into cyclohexylamine salts by reaction with ammonium chloride followed by treatment with cyclohexylamine.
GB17080/40A 1939-11-29 1940-11-29 Improvements in and relating to the preparation of hydroxy dithionaphthoic acids and their derivatives Expired GB551305A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US551305XA 1939-11-29 1939-11-29

Publications (1)

Publication Number Publication Date
GB551305A true GB551305A (en) 1943-02-17

Family

ID=21995816

Family Applications (1)

Application Number Title Priority Date Filing Date
GB17080/40A Expired GB551305A (en) 1939-11-29 1940-11-29 Improvements in and relating to the preparation of hydroxy dithionaphthoic acids and their derivatives

Country Status (1)

Country Link
GB (1) GB551305A (en)

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