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HRID 363710作成日:2026年10月27日

Phthalonitrile → Phthalocyanine

https://huagongshe.com/reaction/363710

反応式

関与物質

役割名称HCID仕込み量
反応物PhthalonitrileHCID 7042—
触媒Titanium TetrachlorideHCID 24193—
溶媒1-ChloronaphthaleneHCID 7003—
生成物PhthalocyanineHCID 86280045—

反応手順

In this comparative example, α-titanyloxyphthalocyanine was prepared by the method disclosed in Japanese Patent Application Laying-open No.62-134651. That is, a mixture of 40 g of phthalodinitrile, 18 g of titanium tetrachloride, and 500 cc of chloronaphthalene was stirred at the temperature of 240° C. to 250° C. for 3 hours in nitrogenous atmosphere to completely react with each other. The mixture was filtrated after the reaction, and as a result dichlorothitanium phthalocyanine was obtained. The obtained dichlorothitanium was mixed with 300 cc of concentrated ammonium solution to obtain a mixture. Then the mixture was heat-refluxed for 1 hour and subjected to the purification by using a Soxhlet extractor. Consequently, titanyloxyphthalocyanine was obtained by drying the purified product. The resultant titanyloxyphthalocyanine was confirmed as α-type crystal having an X-ray diffraction spectrum which is the same as the one shown in FIG. 3.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05874570
出典データセットuspto-grants-1999_02
ORD IDord-22bf60cda7144d808e529c5e8e761ca4
出典メモuspto-grants-1999_02