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HRID 2072330作成日:2026年10月27日

Carbon Dioxide → 2-(3-Phosphonophenylamino)-naphthalene

https://huagongshe.com/reaction/2072330

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物Hydrochloric AcidHCID 313—
反応物Sulfur DioxideHCID 1119—
反応物3-Hydroxy-2-naphthoic acidHCID 7104—
反応物Sodium HydroxideHCID 14798—
反応物Phosphonic acid, P-(3-aminophenyl)-HCID 79477—
反応物Sodium BisulfiteHCID 23665763—
溶媒WaterHCID 962—
生成物2-(3-Phosphonophenylamino)-naphthaleneHCID 21408091—

反応条件

温度80 °C

反応手順

Water (20 parts) is set stirring and 2-hydroxy-3-naphthoic acid (9.5 parts) charged. Sodium hydroxide liquor (70° Tw -- 6.8 parts) is then added until an alkaline reaction is obtained on Brilliant Yellow test paper. 3-aminophenylphosphonic acid (8.7 parts) and sodium bisulphite liquor (40% -- 100 parts) are charged and the mixture is stirred and boiled under reflux for 18 hours. Carbon dioxide is evolved during the early part of the boiling period. After cooling to 80° C the suspension is acidified with hydrochloric acid (36% -- 59 parts) until acid reaction is obtained on Congo Red paper. During acidification the temperature is raised steadily to the boiling point and the suspension is boiled under reflux for 1-2 hours until evolution of sulphur dioxide has essentially ceased. During this period samples are spotted on to Congo Red test paper to confirm a positive acid reaction. The suspension is then cooled to room temperature, filtered and the cake washed with water (10 parts). The paste (18.2 parts) is dried an air at 50° C to give 12.9 parts of 2-(3-phosphonophenylamino)-naphthalene.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04051175
出典データセットuspto-grants-1977_09
ORD IDord-6b520224b72143d4bca35cc20a7a03f9
出典メモuspto-grants-1977_09