GB340262A - Process for the manufacture and production of dibenzanthrones and isodibenzanthronescontaining chlorine and bromine - Google Patents

Process for the manufacture and production of dibenzanthrones and isodibenzanthronescontaining chlorine and bromine

Info

Publication number
GB340262A
GB340262A GB419030A GB419030A GB340262A GB 340262 A GB340262 A GB 340262A GB 419030 A GB419030 A GB 419030A GB 419030 A GB419030 A GB 419030A GB 340262 A GB340262 A GB 340262A
Authority
GB
United Kingdom
Prior art keywords
acid
dyes
bromine
chlorine
product
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
GB419030A
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 GB419030A priority Critical patent/GB340262A/en
Publication of GB340262A publication Critical patent/GB340262A/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
    • C09B3/00Dyes with an anthracene nucleus condensed with one or more carbocyclic rings
    • C09B3/22Dibenzanthrones; Isodibenzanthrones
    • C09B3/30Preparation from starting materials already containing the dibenzanthrone or isodibenzanthrone nucleus
    • C09B3/32Preparation from starting materials already containing the dibenzanthrone or isodibenzanthrone nucleus by halogenation

Landscapes

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

Abstract

Dibenzanthrones and isodibenzanthrones containing substantial amounts of both chlorine and bromine are made by treating parent materials containing one of these halogens with the other halogen, or agents supplying the same, or by treating unhalogenated parent materials simultaneously with both halogens, or agents supplying the same, in the absence of any diluting medium or in any inorganic diluting medium, which may have acid, neutral or alkaline reaction. As inorganic diluting media, water, chlorsulphonic acid, sulphuric acid, oleum, methylsulphuric acid, pyrosulphuric acid, persulphuric acid, phosphoric acid, liquid sulphur dioxide, phosphorus oxychloride, and sulphuryl chloride, and mixtures thereof, are specified. The acid set free during the reaction may be neutralized by addition of alkalies or salts of alkali metals and weak acids, or the concentration of hydrogen ions may be kept constant by the addition of buffer compounds. The usual halogen transferrers, such as iodine, sulphur, selenium or metals and metal compounds, e.g. iron, copper, mercury and antimony, may be employed. Dibenzanthrones and isodibenzanthrones produced by halogenation in organic solvents, or in the absence of solvents, or dibenzanthrones chlorinated in chlorsulphonic acid (Specification 212,145, [Class 2 (iii), Dyes &c.], may be used as parent materials, as well as the bromo derivatives prepared according to Specifications 325,525 and 329,263, [both in Class 2 (iii), Dyes &c.]. The products may be p purified by crystallization or by means of their oxonium salts, or by treating their aqueous pastes with oxidizing agents, e.g. hypochlorites. In examples, (1) the dyestuff obtained by alkylating Bz2 : Bz2'-dihydroxydibenzanthrone with the chlorethyl ester of p-toluenesulphonic acid is brominated in chlorsulphonic acid in presence of antimony; the product, containing chlorine and bromine, dyes fast green blue shades, (2) dichlorisodibenzanthrone, made by treating pure isodibenzanthrone with sulphurylchloride, is brominated in chlorsulphonic acid in the presence of antimony; the product dyes fast blue violet shades, (3) dibenzanthrone is chlorinated with a solution of chlorine in aqueous caustic soda, and bromine is passed into the reaction mixture; the product dyes navy blue shades, (4) dibromdibenzanthrone (made by brominating in nitrobenzene in presence of iron and iodine) is treated with chlorine in dilute oleum; the product dyes navy blue shades, (5) dibenzanthrone is treated with phosphorus pentachloride and bromine in phosphoric acid; the product dyes navy blue shades, (6) 6 : 6'-dichlorisodibenzanthrone, made by alkaline condensation of 6 : Bz1'-dichlorbenzanthrone, is brominated in dilute oleum in presence of arsenic; the product dyes clear blue violet shades, (7) monochlordibenzanthrone (made by chlorination in chlorsulphonic acid in presence of antimony) is ground with bromine in a ball mill; the product dyes fast blue shades, and (8) an aqueous paste of dibenzanthrone is brominated, and the reaction mixture is made weakly alkaline with caustic soda solution and treated with sodium hypochlorite; the product dyes navy blue shades. Specification 284,656, [Class 2 (iii), Dyes &c.], also is referred to.
GB419030A 1929-06-21 1929-06-21 Process for the manufacture and production of dibenzanthrones and isodibenzanthronescontaining chlorine and bromine Expired GB340262A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB419030A GB340262A (en) 1929-06-21 1929-06-21 Process for the manufacture and production of dibenzanthrones and isodibenzanthronescontaining chlorine and bromine

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB419030A GB340262A (en) 1929-06-21 1929-06-21 Process for the manufacture and production of dibenzanthrones and isodibenzanthronescontaining chlorine and bromine

Publications (1)

Publication Number Publication Date
GB340262A true GB340262A (en) 1930-12-22

Family

ID=9772399

Family Applications (1)

Application Number Title Priority Date Filing Date
GB419030A Expired GB340262A (en) 1929-06-21 1929-06-21 Process for the manufacture and production of dibenzanthrones and isodibenzanthronescontaining chlorine and bromine

Country Status (1)

Country Link
GB (1) GB340262A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102660130A (en) * 2012-04-19 2012-09-12 徐州开达精细化工有限公司 Method for producing reductive direct black BCN raw dye

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102660130A (en) * 2012-04-19 2012-09-12 徐州开达精细化工有限公司 Method for producing reductive direct black BCN raw dye

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