GB386997A - Improved manufacture of anthraquinone derivatives - Google Patents
Improved manufacture of anthraquinone derivativesInfo
- Publication number
- GB386997A GB386997A GB2114531A GB2114531A GB386997A GB 386997 A GB386997 A GB 386997A GB 2114531 A GB2114531 A GB 2114531A GB 2114531 A GB2114531 A GB 2114531A GB 386997 A GB386997 A GB 386997A
- Authority
- GB
- United Kingdom
- Prior art keywords
- disulphonate
- halogen
- trihalogenanthraquinones
- halogenanthraquinone
- dichloroanthraquinone
- 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
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/28—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/39—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing halogen atoms bound to the carbon skeleton
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Di - halogenanthraquinone mono - sulphonic acids and trihalogenanthraquinones therefrom are obtained by sulphonating in absence of catalysts, a homonuclear di-halogenanthraquinone in which one halogen atom occupies the 1-position, to give mono-sulphonic acids, which are separated and treated with halogen to give trihalogenanthraquinones. According to examples, 1 : 2, 1 : 3, and 1 : 4 dichloranthraquinones are suphonated in fuming sulphuric acid and the products may be treated with halogen to replace the sulphonic groups in known manner. Specification 373,127 is referred to. The Provisional Specification refers also to the formation of disulphonic acids and is not limited to dihalogen compounds with a halogen atom in the 1-position. In examples 1 : 5 - dichloroanthraquinone is sulphonated with and without a mercury catalyst to yield respectively the 2- and 4-sulphonates and the 2 : 8-disulphonate and the 4-sulphonate and 4 : 8-disulphonate. Sulphonation of 1 : 8-dichloroanthraquinone yielded the 4-sulphonate and the 4 : 5-disulphonate the amount of the latter being increased by adding a mercury catalyst. Chlorination gives the corresponding tri- and tetrachloroanthraquinones.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2114531A GB386997A (en) | 1931-07-24 | 1931-07-24 | Improved manufacture of anthraquinone derivatives |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2114531A GB386997A (en) | 1931-07-24 | 1931-07-24 | Improved manufacture of anthraquinone derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
GB386997A true GB386997A (en) | 1933-01-24 |
Family
ID=10157952
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2114531A Expired GB386997A (en) | 1931-07-24 | 1931-07-24 | Improved manufacture of anthraquinone derivatives |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB386997A (en) |
-
1931
- 1931-07-24 GB GB2114531A patent/GB386997A/en not_active Expired
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