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HRID 2072330생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2072330

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물Hydrochloric AcidHCID 313—
반응물Sulfur DioxideHCID 1119—
반응물3-Hydroxy-2-naphthoic acidHCID 7104—
반응물Sodium HydroxideHCID 14798—
반응물Phosphonic acid, P-(3-aminophenyl)-HCID 79477—
반응물Sodium BisulfiteHCID 23665763—
용매WaterHCID 962—
생성물2-(3-Phosphonophenylamino)-naphthaleneHCID 21408091—

반응 조건

온도80 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04051175
출처 데이터셋uspto-grants-1977_09
ORD IDord-6b520224b72143d4bca35cc20a7a03f9
출처 메모uspto-grants-1977_09