Reaktion #1726336

ord-d50402c8e69a4e6eb11f76c26da85c15

Reaktionsgleichung

c1ccc2c(c1)-c1nc-2nc2[nH]c(nc3nc(nc4[nH]c(n1)c1ccccc41)-c1ccccc1-3)c1ccccc21
phthalocyanine
[O-2].[Ti+4].c1ccc2c(c1)-c1nc3nc(nc4[n-]c(nc5[n-]c(nc-2n1)c1ccccc51)c1ccccc41)-c1ccccc1-3
TiOPc
[Ti].c1ccc2c(c1)-c1nc-2nc2[nH]c(nc3nc(nc4[nH]c(n1)c1ccccc41)-c1ccccc1-3)c1ccccc21
titanium phthalocyanine

Reagenzien

Keine

Reaktionsbedingungen

Temperatur
5°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONthe other material was added, in a proportion
  2. 2
    Sonstigeprepared in Example 1
  3. 3
    workup.ADDITIONmixed together
  4. 4
    workup.STIRRINGwith stirring at a high speed, and crystals
  5. 5
    Sonstigeprecipitated
  6. 6
    Filtrationwere filtrated
  7. 7
    WaschenThe crystals were washed with distilled water until the acid
  8. 8
    Sonstigedried

Vorschrift

The phthalocyanine derivative prepared in Referential Example or the other material was added, in a proportion shown in Table 7, to 10 parts of the TiOPc crude prepared in Example 1, and mixed together and then the mixture was gradually dissolved in 200 parts of 97% sulfuric acid solution at 2° C., and the resulting mixture was stirred for 1 hour with maintaining its temperature at not higher than 5° C. Then, this sulfuric acid solution was slowly poured into 2000 parts of ice water with stirring at a high speed, and crystals precipitated were filtrated. The crystals were washed with distilled water until the acid did not remain, and then dried to give a titanium phthalocyanine compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04882427uspto-grants-1989_11