General Synthesis

Anthraquinone dyes are prepared by the stepwise introduction of substituents onto the preformed anthraquinone skeleton (1) or ring closure of appropriately substituted precursors. The degree of freedom for producing a variety of different structures is restricted, and the availability of only eight substitution centers imposes a further restriction on synthetic flexibility. Therefore, there is signifi­cantly less synthetic versatility than in the case of azo dyes, and consequently less variety; this is a drawback of anthraquinone dyes.

Although tautomerism is theoretically possible in amino and hydroxy anthra­quinone dyes, none has been observed. Studies by 13C NMR spectroscopy have shown convincingly that amino and hydroxy dyes of 9,10-anthraquinone exist as such.

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