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HRID 65545作成日:2026年10月25日

Ammonia → HCID 20233207、化合物

https://huagongshe.com/reaction/65545

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物PhenolHCID 996—
反応物Boric AcidHCID 7628—
反応物1-ChlorohexadecaneHCID 20993—
反応物Hydrazine hydrate (1:1)HCID 24654—
反応物9,10-Anthracenedione, 1-amino-4,5-dihydroxy-8-nitro-HCID 5484079—
反応物HCID 20233208HCID 20233208—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒NitrobenzeneHCID 7416—
生成物HCID 20233207HCID 20233207—

反応条件

温度110 °C

反応手順

120 parts of phenol, 6.1 parts (0.1 mole) of boric acid and 70 parts of toluene are refluxed, while stirring, the water of reaction formed thereby being removed from the system. The toluene is then distilled off, the mixture is cooled to 110° C. and 25.4 parts (0.05 mole) of 1-palmitylamino-8-amino-4,5-dihydroxyanthraquinone (prepared by reacting 1-amino-8-nitro-4,5-dihydroxyanthraquinone with palmityl chloride in nitrobenzene and then reducing the product with hydrazine hydrate) are added. Ammonia is then passed in at this temperature until no further starting material can be detected in the thin-layer chromatogram (duration: 3 hours). The reaction mixture is cooled to 90° C. and 240 parts of methanol are added. After cooling to room temperature, the dye precipitated is filtered off with suction and the material on the filter is washed with methanol and water and dried. 20 parts of 1,4-diamino-5-hydroxy-8-palmitylaminoanthraquinone of melting point 174° C. are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04614804
出典データセットuspto-grants-1986_09
ORD IDord-e81c7b4ace6c436c8bde44d85e7a56a3
出典メモuspto-grants-1986_09