GB206150A - Manufacture of new derivatives of naphthoquinone - Google Patents
Manufacture of new derivatives of naphthoquinoneInfo
- Publication number
- GB206150A GB206150A GB26612/23A GB2661223A GB206150A GB 206150 A GB206150 A GB 206150A GB 26612/23 A GB26612/23 A GB 26612/23A GB 2661223 A GB2661223 A GB 2661223A GB 206150 A GB206150 A GB 206150A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oxynaphthalene
- naphthoquinone
- arylimino
- phenylimino
- naphthoquinones
- 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
- C07C309/45—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton
- C07C309/49—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton the carbon skeleton being further substituted by singly-bound oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Arylimino-2-naphthoquinones, excepting the phenylimino body, are prepared by the process described in the parent Specification by the oxidation in alkaline solution, for example by means of hypochlorites, peroxides or atmospheric oxygen, of 1-arylamino-2-oxynaphthalenes, prepared for example as described in Specification 182,084. An example shows the oxidation by means of cold alkaline hypochlorite of o-methoxyphenyl-1-amino-2-oxynaphthalene, obtained by the action of o-anisidine on a -chlor- or a -brom-b -naphthol. 1-Tolylamino-2-oxynaphthalene and 1-naphthylamino-2-oxynaphthalene may be similarly treated. 1-Arylamino-2-oxynaphthalene sulphonic acids are produced by the action of a normal or acid sulphite upon the 1-arylimino-2-naphthoquinones described above. An example shows the treatment of 1-phenylimino-2-naphthoquinone or any of its homologues or immediate derivatives with sodium bisulphite. The sodium salt thus formed is dissolved in sodium carbonate solution and the free acid liberated by acidification with a mineral acid.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR206150X | 1922-10-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB206150A true GB206150A (en) | 1925-01-15 |
Family
ID=8880407
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB26612/23A Expired GB206150A (en) | 1922-10-28 | 1923-10-24 | Manufacture of new derivatives of naphthoquinone |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB206150A (en) |
-
1923
- 1923-10-24 GB GB26612/23A patent/GB206150A/en not_active Expired
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