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 derivativesInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C327/00—Thiocarboxylic 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.
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) |
-
1940
- 1940-11-29 GB GB17080/40A patent/GB551305A/en not_active Expired
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