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US4294769A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for the preparation of 1,4-diamino-2,3-dicyano-anthraquinones

Assignee: Bayer AG
•
Filing: 1980-07-24
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Granted: 1981-10-13
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Expires: 2000-07-24
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Abstract

Abstract 2,3-Dicyano-anthraquinones of the formula ##STR1## wherein R denotes hydrogen, alkyl or cycloalkyl, are obtained in good yields and high purity by reacting compounds of the formula ##STR2## wherein X denoted hydrogen or the sulphonic acid group, with cyanides in formamide or N-methylformamide as solvents, and if appropriate oxidizing agents and heavy metal catalysts.

Inventors

  • 👤 Friedrich W. Krock
  • 👤 Rutger Neeff
  • 👤 Heinz Scheiter

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-26 11:24
CPC Classifications
C; C09; C09B; C09B1/00; C09B1/16; C09B1/20; C09B1/26; C09B1/28; C09B1/22

Claims Analysis

Total Claims: 11
Claim 1
Independent Claim 65 words
Process for the preparation of 2,3-dicyanoanthraquinones of the formula ##STR9## wherein R denotes hydrogen, optionally substituted alkyl or optionally substituted cycloalkyl, by reacting sulphonic acids of the formula ##STR10## or salts thereof, wherein R has the abovementioned meaning and X denotes hydrogen or the sulphonic acid group, with compounds which donate cyanide ions, characterised in that the reaction is carried out in formamide or N-methyl-formamide.
Claim 2
Dependent Claim 65 words
Process for the preparation of 2,3-dicyanoanthraquinones of the formula ##STR9## wherein R denotes hydrogen, optionally substituted alkyl or optionally substituted cycloalkyl, by reacting sulphonic acids of the formula ##STR10## or salts thereof, wherein R has the abovementioned meaning and X denotes hydrogen or the sulphonic acid group, with compounds which donate cyanide ions, characterised in that the reaction is carried out in formamide or N-methyl-formamide.
Claim 3
Dependent Claim 15 words
Process according to claim 1, characterised in that the reaction is carried out in formamide.
Claim 4
Dependent Claim 28 words
Process according to claim 1, characterised in that the reaction is carried out in the presence of oxidising agents and if appropriate heavy metal catalysts and acid-binding agents.
Claim 5
Dependent Claim 23 words
Process according to claim 3, characterised in that air, oxygen, nitrobenzene or m-nitrobenzenesulphonic acid or salts thereof is used as the oxidising agent.
Claim 6
Dependent Claim 29 words
Process according to claim 3, characterised in that air, in the presence of heavy metal catalysts, such as vanadates, molybdates or copper salts, is used as the oxidising agent.
Claim 7
Dependent Claim 22 words
Process according to claim 1, characterised in that sodium cyanide or potassium cyanide is used as the compound which donates cyanide ions.
Claim 8
Dependent Claim 22 words
Process according to claim 1, characterised in that 1-amino-4-alkylamino-, 1-amino-4-cycloalkylamino- or 1,4-diamino-anthraquinone-2-sulphonic acids or salts thereof are employed as the sulphonic acids.
Claim 9
Dependent Claim 20 words
Process according to claim 1, characterised in that 1,4-diamino-anthraquinone-2-sulphonic acid or a salt thereof is employed as the sulphonic acid.
Claim 10
Dependent Claim 20 words
Process according to claim 1, characterised in that 1,4-diamino-anthraquinone-2,3-disulphonic acid or a salt thereof is employed as the sulphonic acid.
Claim 11
Dependent Claim 17 words
Dicyano-anthraquinone dyestuffs of the formula given in claim 1, wherein R denotes an optionally substituted cycloalkyl radical.

References Cited (Backward Citations)

US1938029A Cited
DE1906834U Cited
US4042605A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1984-10-12 1985-04-13 1985-10-13 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1988-10-12 1989-04-13 1989-10-13 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1992-10-12 1993-04-13 1993-10-13 $7700.00 Window Closed / Lapsed

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