GB322209A - Improvements in the manufacture and production of azine derivatives - Google Patents

Improvements in the manufacture and production of azine derivatives

Info

Publication number
GB322209A
GB322209A GB2461028A GB2461028A GB322209A GB 322209 A GB322209 A GB 322209A GB 2461028 A GB2461028 A GB 2461028A GB 2461028 A GB2461028 A GB 2461028A GB 322209 A GB322209 A GB 322209A
Authority
GB
United Kingdom
Prior art keywords
dinaphthazine
derivatives
sulphonic acid
heated
dilute caustic
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
GB2461028A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to GB2461028A priority Critical patent/GB322209A/en
Publication of GB322209A publication Critical patent/GB322209A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B17/00Azine dyes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Indole Compounds (AREA)

Abstract

322,209. Johnson, J. Y., (I. G. Farbenindustrie Akt.-Ges.). Aug. 27, 1928. Naphthazine derivatives.-The sulphonic acid derivatives of 1: 2-naphthophenazine and of 1 : 2 : 1<1> : 2'-dinaphthazine are converted to the corresponding hydroxy derivatives by heating with dilute caustic alkali solutions containing up to 10 per cent of caustic alkali. The reaction is preferably carried out under pressure and may be effected together with the production of the starting material in one operation. Generally, the use of the theoretical quantity of alkali is sufficient. In examples, the sodium salts of 1:2:1<1>:2<1>-dinaphthazine-8 : 8<1>- and 5: 5<1>-disulphonic acids and of 1 : 2-naphthophenazine-6- sulphonic acid (obtained from 1.2-naphthoquinone and o-phenylene diamine) are heated with dilute caustic soda lye to yield the corresponding hydroxy derivatives. The sodium salt of 2- naphthylamine-8-sulphonic acid is first heated with a solution of sodium hydroxide and hypochlorite and the resulting dinaphthazine, after further diluting the solution, is heated under pressure to give 8: 8<1>-dihydroxy-1: 2 : 1<1> : 2'-dinaphthazine. The Provisional Specification refers also to the treatment of any azine sulphonic acids with dilute caustic alkalis.
GB2461028A 1928-08-27 1928-08-27 Improvements in the manufacture and production of azine derivatives Expired GB322209A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2461028A GB322209A (en) 1928-08-27 1928-08-27 Improvements in the manufacture and production of azine derivatives

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2461028A GB322209A (en) 1928-08-27 1928-08-27 Improvements in the manufacture and production of azine derivatives

Publications (1)

Publication Number Publication Date
GB322209A true GB322209A (en) 1929-11-27

Family

ID=10214366

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2461028A Expired GB322209A (en) 1928-08-27 1928-08-27 Improvements in the manufacture and production of azine derivatives

Country Status (1)

Country Link
GB (1) GB322209A (en)

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